Item 42 of 56 (back to results) previous next   Toxins, Biological D014118               MeSH Unique Identifier: D014118 Scope Notes: Specific, characterizable, poisonous chemicals, often PROTEINS, with specific biological properties, including immunogenicity, produced by microbes, higher plants (PLANTS, TOXIC), or ANIMALS. Click here for more information

Current search: C17. Skin and Connective Tissue Diseases: Skin Diseases [MESH:D012871] > Nail Diseases [MESH:D009260] > Pachyonychia Congenita [MESH:D053549] > Steatocystoma Multiplex [MESH:D062685] × Select any link to see items in a related category. more general categories    information about this item A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Lower Extremity [MESH:D035002] (139)   Foot [MESH:D005528] (125)   Forefoot, Human [MESH:D005545] (118)   Toes [MESH:D014034] (115)   Synpolydactyly 1 [MESH:C566094] (11)  Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Synpolydactyly 1 [MESH:C566094] (11)  Head [MESH:D006257] (523)   Face [MESH:D005145] (387)   Frontonasal dysplasia [MESH:C538065] (52)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Leg Bones [MESH:D007867] (228)   Femur [MESH:D005269] (52)   Acrocapitofemoral Dysplasia [MESH:C564334] (39)  Bones of Upper Extremity [MESH:D001133] (240)   Arm Bones [MESH:D050280] (183)   Radius [MESH:D011884] (126)   VATER association [MESH:C536534] (46)  Skull [MESH:D012886] (610)   Facial Bones [MESH:D005147] (539)   Jaw [MESH:D007568] (524)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Spine [MESH:D013131] (258)   VATER association [MESH:C536534] (46)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Mouth [MESH:D009055] (60)   Salivary Glands [MESH:D012469] (51)   Aplasia of Lacrimal and Salivary Glands [MESH:C562407] (42)  Upper Gastrointestinal Tract [MESH:D041742] (236)   Esophagus [MESH:D004947] (200)   VATER association [MESH:C536534] (46)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Pancreas [MESH:D010179] (61)   Pancreatic Agenesis, Congenital [MESH:C564908] (44)  Respiratory System [MESH:D012137] (321)   Trachea [MESH:D014132] (190)   VATER association [MESH:C536534] (46)  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   Nephrons [MESH:D009399] (518)   Kidney Tubules [MESH:D007684] (510)   Kidney Tubules, Proximal [MESH:D007687] (504)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Atria [MESH:D006325] (65)   Atrial Standstill [MESH:C563984] (32)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Ear, Inner [MESH:D007758] (43)   Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia [MESH:C565195] (11)  Eye [MESH:D005123] (858)   Lacrimal Apparatus [MESH:D007765] (48)   Aplasia of Lacrimal and Salivary Glands [MESH:C562407] (42)  Tissues [MESH:D014024] (397)   Exocrine Glands [MESH:D005088] (88)   Lacrimal Apparatus [MESH:D007765] (45)   Aplasia of Lacrimal and Salivary Glands [MESH:C562407] (42)  Salivary Glands [MESH:D012469] (51)   Aplasia of Lacrimal and Salivary Glands [MESH:C562407] (42)  Sweat Glands [MESH:D013545] (26)   Eccrine Glands [MESH:D004439] (23)   Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  Stomatognathic System [MESH:D013284] (673)   Jaw [MESH:D007568] (528)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Mouth [MESH:D009055] (194)   Dentition [MESH:D003817] (109)   Tooth [MESH:D014070] (61)   Incisor [MESH:D007180] (51)   Single upper central incisor [MESH:C537342] (50)  Salivary Glands [MESH:D012469] (51)   Aplasia of Lacrimal and Salivary Glands [MESH:C562407] (42)  Embryonic Structures [MESH:D004628] (139)   Mullerian Ducts [MESH:D009095] (65)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  Integumentary System [MESH:D034582] (104)   Skin [MESH:D012867] (57)   Sweat Glands [MESH:D013545] (26)   Eccrine Glands [MESH:D004439] (23)   Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Bacteremia [MESH:D016470] (208)  Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Helicobacter Infections [MESH:D016481] (579)  Pasteurellaceae Infections [MESH:D016871] (348)  Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Neisseriaceae Infections [MESH:D016870] (273)   Meningococcal Infections [MESH:D008589] (242)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Staphylococcal Infections [MESH:D013203] (264)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Leprosy [MESH:D007918] (261)  Paratuberculosis [MESH:D010283] (427)  Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)   Atypical Mycobacteriosis, Familial, X-Linked 1 [MESH:C567070] (56)  Tuberculosis [MESH:D014376] (992)   Tuberculosis, Pulmonary [MESH:D014397] (678)  Streptococcal Infections [MESH:D013290] (158)   Pneumococcal Infections [MESH:D011008] (122)   Invasive Pneumococcal Disease, Recurrent Isolated, 1 [MESH:C563662] (35)  Invasive Pneumococcal Disease, Recurrent Isolated, 2 [MESH:C564468] (56)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Urinary Tract Infections [MESH:D014552] (984)  Eye Infections [MESH:D015817] (86)   Corneal Ulcer [MESH:D003320] (61)  Intraabdominal Infections [MESH:D059413] (958)   Appendicitis [MESH:D001064] (774)  Peritonitis [MESH:D010538] (800)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Skin Diseases, Infectious [MESH:D012874] (415)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289)  Mycoses [MESH:D009181] (385)   Candidiasis [MESH:D002177] (307)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Pneumonia, Viral [MESH:D011024] (125)  Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Herpesviridae Infections [MESH:D006566] (1944)   Cytomegalovirus Infections [MESH:D003586] (222)  Sarcoma, Kaposi [MESH:D012514] (1578)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Papillomavirus Infections [MESH:D030361] (630)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  RNA Virus Infections [MESH:D012327] (4215)   Arenaviridae Infections [MESH:D001117] (204)   Lassa Fever [MESH:D007835] (38)  Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Hemorrhagic Fevers, Viral [MESH:D006482] (102)   Lassa Fever [MESH:D007835] (38)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Nidovirales Infections [MESH:D030341] (136)   Coronaviridae Infections [MESH:D003333] (133)   Coronavirus Infections [MESH:D018352] (131)   Severe Acute Respiratory Syndrome [MESH:D045169] (127)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Skin Diseases, Viral [MESH:D017193] (203)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Slow Virus Diseases [MESH:D012897] (782)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  Tumor Virus Infections [MESH:D014412] (1069)   Papillomavirus Infections [MESH:D030361] (537)  Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Protozoan Infections [MESH:D011528] (3014)   Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Malaria [MESH:D008288] (2175)   Malaria, Falciparum [MESH:D016778] (438)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Leukemia, T-Cell [MESH:D015458] (395)   Leukemia-Lymphoma, Adult T-Cell [MESH:D015459] (138)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphatic Vessel Tumors [MESH:D018190] (171)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Extranodal NK-T-Cell [MESH:D054391] (132)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Hepatoblastoma [MESH:D018197] (548)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Liposarcoma [MESH:D008080] (612)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Cutaneous [MESH:D034701] (45)  Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Aggressive [MESH:D018222] (1562)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Leiomyosarcoma [MESH:D007890] (977)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Leiomyosarcoma [MESH:D007890] (977)  Liposarcoma [MESH:D008080] (612)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Kaposi [MESH:D012514] (1578)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Adenoma, Liver Cell [MESH:D018248] (685)  Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adrenocortical Carcinoma [MESH:D018268] (821)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Lobular [MESH:D018275] (305)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Pilomatrixoma [MESH:D018296] (252)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Lobular [MESH:D018275] (305)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Sarcoma, Kaposi [MESH:D012514] (1578)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioma, capillary infantile [MESH:C535860] (190)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Nevus [MESH:D009506] (340)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neoplasms by Site [MESH:D009371] (9169)   Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Facial Neoplasms [MESH:D005153] (27)   Eyelid Neoplasms [MESH:D005142] (25)   Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Nose Neoplasms [MESH:D009669] (390)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Hematologic Neoplasms [MESH:D019337] (104)   Bone Marrow Neoplasms [MESH:D019046] (91)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Vaginal Neoplasms [MESH:D014625] (363)  Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Wilms Tumor [MESH:D009396] (553)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Precancerous Conditions [MESH:D011230] (2858)   Aberrant Crypt Foci [MESH:D058739] (326)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Warts [MESH:D014860] (167)   WHIM syndrome [MESH:C536697] (148) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Cartilage Diseases [MESH:D002357] (438)  Bone Diseases [MESH:D001847] (5801)   Osteitis Deformans [MESH:D010001] (287)  Osteonecrosis [MESH:D010020] (539)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromicric dysplasia [MESH:C535662] (520)  Acrocapitofemoral Dysplasia [MESH:C564334] (39)  Marfan Syndrome [MESH:D008382] (646)  Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Dwarfism [MESH:D004392] (778)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)   Hypertelorism [MESH:D006972] (109)   Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Syndactyly, type v [MESH:C538155] (11)  Brachydactyly-Syndactyly Syndrome [MESH:C565193] (11)  Synpolydactyly 1 [MESH:C566094] (11)  Osteochondrodysplasias [MESH:D010009] (2440)   Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Fibrous Dysplasia of Bone [MESH:D005357] (737)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Osteosclerosis [MESH:D010026] (356)   Osteopetrosis [MESH:D010022] (318)   Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Bone Diseases, Endocrine [MESH:D001849] (747)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)   Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Hyperostosis [MESH:D015576] (493)   Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)   Intervertebral disc disease [MESH:C535531] (514)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Hand foot uterus syndrome [MESH:C535627] (20)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Hand foot uterus syndrome [MESH:C535627] (20)  Jaw Diseases [MESH:D007571] (1601)   Mandibular Diseases [MESH:D008336] (395)  Maxillary Diseases [MESH:D008439] (354)  Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Joint Diseases [MESH:D007592] (4657)   Calcification of Joints and Arteries [MESH:C565891] (60)  Arthralgia [MESH:D018771] (191)  Ankylosis [MESH:D000844] (479)   Spondylitis, Ankylosing [MESH:D013167] (431)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Arthrogryposis [MESH:D001176] (329)   Distal arthrogryposis type 2B [MESH:C538400] (85)  Lethal Congenital Contracture Syndrome 2 [MESH:C564369] (85)  Muscular Diseases [MESH:D009135] (4071)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Muscle Rigidity [MESH:D009127] (617)  Muscle Spasticity [MESH:D009128] (187)  Muscle Weakness [MESH:D018908] (478)  Arthrogryposis [MESH:D001176] (329)   Distal arthrogryposis type 2B [MESH:C538400] (85)  Lethal Congenital Contracture Syndrome 2 [MESH:C564369] (85)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 4 [MESH:C538351] (47)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Arthrogryposis [MESH:D001176] (329)   Distal arthrogryposis type 2B [MESH:C538400] (85)  Lethal Congenital Contracture Syndrome 2 [MESH:C564369] (85)  Craniofacial Abnormalities [MESH:D019465] (3098)   Craniofrontonasal dysplasia [MESH:C536456] (36)  Frontonasal dysplasia [MESH:C538065] (52)  Costello Syndrome [MESH:D056685] (407)  Craniosynostoses [MESH:D003398] (438)  Donohue Syndrome [MESH:D056731] (95)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Microcephaly [MESH:D008831] (700)  Silver-Russell Syndrome [MESH:D056730] (142)  Craniofacial Dysostosis [MESH:D003394] (391)   Hypertelorism [MESH:D006972] (109)   Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 5 [MESH:C548083] (169)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Chondrodysplasia, acromesomelic, with genital anomalies [MESH:C537913] (20)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Brachydactyly [MESH:D059327] (220)   Brachydactyly type A1 [MESH:C537088] (39)  Brachydactyly type A2 [MESH:C537089] (28)  Brachydactyly, Type D [MESH:C562420] (11)  Acrocapitofemoral Dysplasia [MESH:C564334] (39)  Brachydactyly-Syndactyly Syndrome [MESH:C565193] (11)  Ectromelia [MESH:D004480] (108)   Tetra-amelia autosomal recessive [MESH:C536498] (19)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Hand foot uterus syndrome [MESH:C535627] (20)  Polydactyly [MESH:D017689] (318)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Syndactyly, type v [MESH:C538155] (11)  Brachydactyly-Syndactyly Syndrome [MESH:C565193] (11)  Synpolydactyly 1 [MESH:C566094] (11)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Hand foot uterus syndrome [MESH:C535627] (20)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Syndactyly, type v [MESH:C538155] (11)  Brachydactyly-Syndactyly Syndrome [MESH:C565193] (11)  Synpolydactyly 1 [MESH:C566094] (11)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Cholelithiasis [MESH:D002769] (373)   Gallstones [MESH:D042882] (350)  Gallbladder Diseases [MESH:D005705] (1215)   Cholecystolithiasis [MESH:D041761] (353)   Gallstones [MESH:D042882] (350)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Hirschsprung Disease [MESH:D006627] (361)  Anus, Imperforate [MESH:D001006] (140)   VATER association [MESH:C536534] (46)  Digestive System Neoplasms [MESH:D004067] (7493)   Gastrointestinal Neoplasms [MESH:D005770] (6460)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Stenosis [MESH:D004940] (490)  Deglutition Disorders [MESH:D003680] (1538)   Esophageal Motility Disorders [MESH:D015154] (1489)   Gastroesophageal Reflux [MESH:D005764] (1465)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Esophagitis [MESH:D004941] (1120)   Esophagitis, Peptic [MESH:D004942] (709)  Gastroenteritis [MESH:D005759] (4066)   Appendicitis [MESH:D001064] (774)  Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enteritis [MESH:D004751] (157)   Ileitis [MESH:D007079] (137)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Esophagitis [MESH:D004941] (1120)   Esophagitis, Peptic [MESH:D004942] (709)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43)  Inflammatory Bowel Disease 14 [MESH:C567383] (22)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Intestinal Diseases [MESH:D007410] (6206)   Intestinal Perforation [MESH:D007416] (471)  Cecal Diseases [MESH:D002429] (1330)   Appendicitis [MESH:D001064] (774)  Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colonic Diseases, Functional [MESH:D003109] (439)   Irritable Bowel Syndrome [MESH:D043183] (429)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enteritis [MESH:D004751] (157)   Ileitis [MESH:D007079] (137)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Ileal Diseases [MESH:D007077] (143)   Ileitis [MESH:D007079] (137)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43)  Inflammatory Bowel Disease 14 [MESH:C567383] (22)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Malabsorption Syndromes [MESH:D008286] (492)   Diarrhea 5, With Tufting Enteropathy, Congenital [MESH:C567703] (70)  Celiac Disease [MESH:D002446] (340)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Esophagitis, Peptic [MESH:D004942] (709)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatic Veno-Occlusive Disease [MESH:D006504] (208)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hypertension, Portal [MESH:D006975] (869)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis C, Chronic [MESH:D019698] (142)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Liver Cirrhosis [MESH:D008103] (5542)   Cirrhosis, Familial [MESH:C566123] (179)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatic Agenesis, Congenital [MESH:C564908] (44)  Cystic Fibrosis [MESH:D003550] (760)  Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Peritoneal Diseases [MESH:D010532] (1119)   Peritoneal Fibrosis [MESH:D056627] (488)  Peritonitis [MESH:D010538] (800) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Mandibular Diseases [MESH:D008336] (450)  Maxillary Diseases [MESH:D008439] (354)  Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  PCI 5002 [MESH:C568608] (527)  Periapical Diseases [MESH:D010483] (186)   Periapical Periodontitis [MESH:D010485] (183)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   PCI 5002 [MESH:C568608] (433)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   PCI 5002 [MESH:C568608] (433)  Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Periodontal Diseases [MESH:D010510] (1001)   Gingival Diseases [MESH:D005882] (217)   Gingival Overgrowth [MESH:D019214] (192)   Gingival Hyperplasia [MESH:D005885] (161)  Periapical Diseases [MESH:D010483] (186)   Periapical Periodontitis [MESH:D010485] (183)  Periodontitis [MESH:D010518] (843)   Periodontitis, Aggressive, 2 [MESH:C566946] (310)  Periapical Periodontitis [MESH:D010485] (183)  Salivary Gland Diseases [MESH:D012466] (1213)   Aplasia of Lacrimal and Salivary Glands [MESH:C562407] (42)  Sialorrhea [MESH:D012798] (252)  Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 12 [MESH:C567548] (434)  Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia [MESH:C565195] (11)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Type IV [MESH:C566293] (8)  Odontodysplasia [MESH:D018126] (24)   Odontoonychodermal dysplasia [MESH:C537742] (21)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia [MESH:C565195] (11)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Type IV [MESH:C566293] (8)  Odontodysplasia [MESH:D018126] (24)   Odontoonychodermal dysplasia [MESH:C537742] (21) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Respiratory System Abnormalities [MESH:D015619] (243)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Laryngeal Diseases [MESH:D007818] (215)   Laryngo onycho cutaneous syndrome [MESH:C537032] (49)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Pulmonary Veno-Occlusive Disease [MESH:D011668] (55)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Hypertension, Pulmonary [MESH:D006976] (2000)   Pulmonary arterial hypertension [MESH:C536282] (94)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Alveolitis, Extrinsic Allergic [MESH:D000542] (496)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Pneumonia, Viral [MESH:D011024] (125)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)   Spinal muscular atrophy with respiratory distress 1 [MESH:C536880] (15)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Cough [MESH:D003371] (179)  Hyperventilation [MESH:D006985] (654)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)   Spinal muscular atrophy with respiratory distress 1 [MESH:C536880] (15)  Respiratory Insufficiency [MESH:D012131] (841)   Hypoventilation [MESH:D007040] (360)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Severe Acute Respiratory Syndrome [MESH:D045169] (127)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Pneumonia, Viral [MESH:D011024] (125)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Nose Neoplasms [MESH:D009669] (390)  Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness [MESH:D003638] (623)   Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Barakat syndrome [MESH:C537907] (71)  Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Deafness, Autosomal Recessive 37 [MESH:C564331] (35)  Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia [MESH:C565195] (11)  Deafness, Autosomal Dominant 20 [MESH:C565754] (69)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 2B [MESH:C567214] (18)  Deafness, Autosomal Dominant 2A [MESH:C567441] (36)  Laryngeal Diseases [MESH:D007818] (211)   Laryngo onycho cutaneous syndrome [MESH:C537032] (49)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Nose Neoplasms [MESH:D009669] (390)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Chronobiology Disorders [MESH:D021081] (970)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Brain Neoplasms [MESH:D001932] (2764)  Basal Ganglia Diseases [MESH:D001480] (4268)   Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)  Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease, Secondary [MESH:D010302] (327)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Cerebellar Diseases [MESH:D002526] (736)   Dandy-Walker Syndrome [MESH:D003616] (50)  Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Cerebrovascular Disorders [MESH:D002561] (5542)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Artery Thrombosis [MESH:D002341] (138)  Carotid Stenosis [MESH:D016893] (174)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Huntington Disease [MESH:D006816] (540)  Lewy Body Disease [MESH:D020961] (1143)  Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)   Frontotemporal Dementia [MESH:D057180] (300)   Pick Disease of the Brain [MESH:D020774] (184)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Unverricht-Lundborg Syndrome [MESH:D020194] (65)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)   Migraine without Aura [MESH:D020326] (408)  Hydrocephalus [MESH:D006849] (276)   Dandy-Walker Syndrome [MESH:D003616] (50)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Hypopituitarism [MESH:D007018] (732)   Panhypopituitarism X-linked [MESH:C538613] (18)  Mental Retardation, X-Linked, With Panhypopituitarism [MESH:C567485] (18)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)   Dandy-Walker Syndrome [MESH:D003616] (50)  Leukoencephalopathies [MESH:D056784] (1916)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Neuroaxonal Dystrophies [MESH:D019150] (100)   Neurodegeneration Due To Cerebral Folate Transport Deficiency [MESH:C567791] (53)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis [MESH:D008581] (1506)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Movement Disorders [MESH:D009069] (4823)   Guanidinoacetate methyltransferase deficiency [MESH:C537622] (60)  Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)  Dystonic Disorders [MESH:D020821] (729)   Myoclonic dystonia [MESH:C536096] (245)  Dystonia, Dopa-responsive [MESH:C538007] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease, Secondary [MESH:D010302] (327)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal muscular atrophy with respiratory distress 1 [MESH:C536880] (15)  Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Nervous System Malformations [MESH:D009421] (3354)   Dandy-Walker Syndrome [MESH:D003616] (50)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 2, X-linked [MESH:C536857] (37)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Neuronal Migration Disorders [MESH:D054081] (264)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Encephalocele [MESH:D004677] (151)   Parietal Foramina 2 [MESH:C566510] (9)  Parietal Foramina [MESH:C566826] (42)  Nervous System Neoplasms [MESH:D009423] (3073)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neurodegenerative Diseases [MESH:D019636] (6613)   Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)  Lewy Body Disease [MESH:D020961] (1143)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)  Rett Syndrome [MESH:D015518] (143)  Unverricht-Lundborg Syndrome [MESH:D020194] (65)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 2, X-linked [MESH:C536857] (37)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal muscular atrophy with respiratory distress 1 [MESH:C536880] (15)  Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)   Guanidinoacetate methyltransferase deficiency [MESH:C537622] (60)  Consciousness Disorders [MESH:D003244] (680)   Unconsciousness [MESH:D014474] (660)   Coma [MESH:D003128] (524)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Mental Retardation, X-Linked, With Panhypopituitarism [MESH:C567485] (18)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Rett Syndrome [MESH:D015518] (143)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Spasm [MESH:D013035] (418)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Muscle Spasticity [MESH:D009128] (187)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Pain, Intractable [MESH:D010148] (707)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2043)   Quadriplegia [MESH:D011782] (115)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Reflex, Abnormal [MESH:D012021] (485)   Reflex, Babinski [MESH:D001405] (97)  Sensation Disorders [MESH:D012678] (5011)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness [MESH:D003638] (623)   Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Barakat syndrome [MESH:C537907] (71)  Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Deafness, Autosomal Recessive 37 [MESH:C564331] (35)  Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia [MESH:C565195] (11)  Deafness, Autosomal Dominant 20 [MESH:C565754] (69)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 2B [MESH:C567214] (18)  Deafness, Autosomal Dominant 2A [MESH:C567441] (36)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal muscular atrophy with respiratory distress 1 [MESH:C536880] (15)  Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Spinal muscular atrophy with respiratory distress 1 [MESH:C536880] (15)  Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Diseases [MESH:D009135] (3538)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 4 [MESH:C538351] (47)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Myasthenic Syndromes, Congenital [MESH:D020294] (155)   Myopathy, Congenital, Compton-North [MESH:C567261] (35)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)   Neuralgia, Postherpetic [MESH:D051474] (742)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 2, X-linked [MESH:C536857] (37)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)  Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Conjunctival Diseases [MESH:D003229] (273)   Laryngo onycho cutaneous syndrome [MESH:C537032] (49)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Keratoconus [MESH:D007640] (121)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Keratitis [MESH:D007634] (168)   Corneal Ulcer [MESH:D003320] (61)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Leber Congenital Amaurosis [MESH:D057130] (157)  Albinism [MESH:D000417] (258)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Retinitis Pigmentosa 7 [MESH:C564284] (8)  Eye Infections [MESH:D015817] (110)   Corneal Ulcer [MESH:D003320] (61)  Eye Neoplasms [MESH:D005134] (413)   Eyelid Neoplasms [MESH:D005142] (25)   Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Eyelid Diseases [MESH:D005141] (882)   Eyelid Neoplasms [MESH:D005142] (25)   Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Aplasia of Lacrimal and Salivary Glands [MESH:C562407] (42)  Dry Eye Syndromes [MESH:D015352] (533)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Cerulean cataract [MESH:C537955] (14)  Alpha-B Crystallinopathy [MESH:C563848] (135)  Cataract, Coppock-Like [MESH:C565133] (20)  Cataract, Pulverulent, Juvenile-Onset [MESH:C565703] (69)  Cataract, Zonular Pulverulent 3 [MESH:C566608] (20)  Cataract, Cortical, Juvenile-Onset [MESH:C566955] (5)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma, Open-Angle [MESH:D005902] (1281)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)  Refractive Errors [MESH:D012030] (457)   Myopia [MESH:D009216] (349)  Retinal Diseases [MESH:D012164] (3747)   Fundus Albipunctatus [MESH:C562733] (47)  Diabetic Retinopathy [MESH:D003930] (1371)  Leber Congenital Amaurosis [MESH:D057130] (157)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinal Degeneration [MESH:D012162] (2386)   Hyaloideoretinal degeneration of Wagner [MESH:C536075] (135)  Macular Degeneration [MESH:D008268] (995)   Fundus Dystrophy, Pseudoinflammatory, Of Sorsby [MESH:C564992] (121)  Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Macular Degeneration, Age-Related, 9 [MESH:C566958] (149)  Macular Degeneration, Age-Related, 11 [MESH:C567450] (61)  Choroidal Dystrophy, Central Areolar 2 [MESH:C567750] (8)  Macular Edema [MESH:D008269] (557)  Retinal Dystrophies [MESH:D058499] (1315)   Patterned dystrophy of retinal pigment epithelium [MESH:C536309] (8)  Retinitis Pigmentosa [MESH:D012174] (1307)   Retinitis Pigmentosa 7 [MESH:C564284] (8)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Aromatase deficiency [MESH:C537436] (277)  Oligospermia [MESH:D009845] (799)  Penile Diseases [MESH:D010409] (1805)   Penile Induration [MESH:D010411] (495)  Penile Neoplasms [MESH:D010412] (890)  Hypospadias [MESH:D007021] (798)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Hyperplasia [MESH:D011470] (336)  Prostatitis [MESH:D011472] (424)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Urogenital Abnormalities [MESH:D014564] (2065)   Hand foot uterus syndrome [MESH:C535627] (20)  Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Aromatase deficiency [MESH:C537436] (277)  Hyperandrogenism [MESH:D017588] (98)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Adrenogenital Syndrome [MESH:D047808] (715)   Hyperandrogenism [MESH:D017588] (98)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  Gonadal Dysgenesis [MESH:D006059] (492)   Ovarian Dysgenesis 2 [MESH:C564499] (15)  Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Lipoprotein Glomerulopathy [MESH:C567089] (165)  Diabetic Nephropathies [MESH:D003928] (2301)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Barakat syndrome [MESH:C537907] (71)  Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Chondrodysplasia, acromesomelic, with genital anomalies [MESH:C537913] (20)  Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Uterine Diseases [MESH:D014591] (2479)   Endometrial Hyperplasia [MESH:D004714] (263)  Uterine Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Vaginal Diseases [MESH:D014623] (446)   Vaginal Neoplasms [MESH:D014625] (363)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Abnormalities [MESH:D014564] (2043)   Hand foot uterus syndrome [MESH:C535627] (20)  Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Aromatase deficiency [MESH:C537436] (277)  Hyperandrogenism [MESH:D017588] (98)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Adrenogenital Syndrome [MESH:D047808] (715)   Hyperandrogenism [MESH:D017588] (98)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  Gonadal Dysgenesis [MESH:D006059] (492)   Ovarian Dysgenesis 2 [MESH:C564499] (15)  Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Vaginal Neoplasms [MESH:D014625] (363)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Lipoprotein Glomerulopathy [MESH:C567089] (165)  Diabetic Nephropathies [MESH:D003928] (2301)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Barakat syndrome [MESH:C537907] (71)  Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Pregnancy Complications [MESH:D011248] (4768)   Diabetes, Gestational [MESH:D016640] (1157)  Fetal Death [MESH:D005313] (464)  Placenta Diseases [MESH:D010922] (1781)  Polyhydramnios [MESH:D006831] (123)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Abortion, Spontaneous [MESH:D000022] (2780)   Embryo Loss [MESH:D020964] (288)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VATER association [MESH:C536534] (46)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Tetralogy of Fallot [MESH:D013771] (121)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 [MESH:C566471] (47)  Heart Septal Defects [MESH:D006343] (385)   Aortopulmonary Septal Defect [MESH:D001028] (47)   Truncus Arteriosus, Persistent [MESH:D014339] (45)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 5 [MESH:C548083] (169)  Vascular Malformations [MESH:D054079] (1098)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Heart Diseases [MESH:D006331] (8614)   Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial fibrillation, familial 1 [MESH:C538261] (32)  Heart Block [MESH:D006327] (571)   Atrial Standstill [MESH:C563984] (32)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 2a [MESH:C567505] (51)  Cardiomyopathy, Dilated, 1z [MESH:C567506] (41)  Cardiomyopathy, Dilated, 1FF [MESH:C567654] (51)  Cardiomyopathies [MESH:D009202] (5331)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Atrial Standstill [MESH:C563984] (32)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Endomyocardial Fibrosis [MESH:D004719] (521)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 [MESH:C566471] (47)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 2a [MESH:C567505] (51)  Cardiomyopathy, Dilated, 1z [MESH:C567506] (41)  Cardiomyopathy, Dilated, 1FF [MESH:C567654] (51)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 13 [MESH:C567686] (41)  Cardiomyopathy, Restrictive [MESH:D002313] (94)   Cardiomyopathy, Familial Restrictive, 1 [MESH:C566168] (51)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VATER association [MESH:C536534] (46)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Tetralogy of Fallot [MESH:D013771] (121)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 [MESH:C566471] (47)  Heart Septal Defects [MESH:D006343] (385)   Aortopulmonary Septal Defect [MESH:D001028] (47)   Truncus Arteriosus, Persistent [MESH:D014339] (45)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 5 [MESH:C548083] (169)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Thrombosis [MESH:D003328] (255)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Calcification of Joints and Arteries [MESH:C565891] (60)  Hepatic Veno-Occlusive Disease [MESH:D006504] (208)  Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Pulmonary Veno-Occlusive Disease [MESH:D011668] (55)  Retinal Vein Occlusion [MESH:D012170] (607)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)  Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Carotid Stenosis [MESH:D016893] (174)  Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebrovascular Disorders [MESH:D002561] (5541)   Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Artery Thrombosis [MESH:D002341] (138)  Carotid Stenosis [MESH:D016893] (174)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Carotid Artery Thrombosis [MESH:D002341] (138)  Intracranial Thrombosis [MESH:D020767] (481)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Carotid Artery Thrombosis [MESH:D002341] (138)  Intracranial Thrombosis [MESH:D020767] (481)  Thrombosis [MESH:D013927] (3101)   Coronary Thrombosis [MESH:D003328] (255)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Carotid Artery Thrombosis [MESH:D002341] (138)  Intracranial Thrombosis [MESH:D020767] (481)  Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Pregnancy-Induced [MESH:D046110] (397)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Thrombosis [MESH:D003328] (255)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  No-Reflow Phenomenon [MESH:D054318] (277)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Telangiectasis [MESH:D013684] (255)   Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784)  Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Purpura, Schoenlein-Henoch [MESH:D011695] (266) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Z. Exceptions (453)   Not Fully Specified [NFS] (453)  Hematologic Diseases [MESH:D006402] (6174)   Pancytopenia [MESH:D010198] (332)  Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 4 [MESH:C567281] (30)  Anemia, Hemolytic [MESH:D000743] (3083)   Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to [MESH:C565545] (88)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemoglobinuria, Paroxysmal [MESH:D006457] (293)   Bone Marrow failure syndromes [MESH:C536572] (248)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Anemia, Macrocytic [MESH:D000748] (382)   5q- syndrome [MESH:C535323] (131)  Anemia, Megaloblastic [MESH:D000749] (288)  Red-Cell Aplasia, Pure [MESH:D012010] (183)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 4 [MESH:C567281] (30)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Antithrombin III Deficiency [MESH:D020152] (80)  Thrombasthenia [MESH:D013915] (98)  Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Thrombasthenia [MESH:D013915] (98)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Thrombocytopenia [MESH:D013921] (2966)   Congenital amegakaryocytic thrombocytopenia [MESH:C535982] (11)  Thrombocytopenia, Neonatal Alloimmune [MESH:D054098] (79)  Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Antithrombin III Deficiency [MESH:D020152] (80)  Hypergammaglobulinemia [MESH:D006942] (137)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Bone Marrow Neoplasms [MESH:D019046] (91)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 4 [MESH:C567281] (30)  Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Hemoglobinuria, Paroxysmal [MESH:D006457] (293)   Bone Marrow failure syndromes [MESH:C536572] (248)  Myeloproliferative Disorders [MESH:D009196] (1492)   Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134)  Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hematologic Neoplasms [MESH:D019337] (104)   Bone Marrow Neoplasms [MESH:D019046] (91)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemorrhagic Disorders [MESH:D006474] (3359)   Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328)  Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombasthenia [MESH:D013915] (98)  Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Leukocyte Disorders [MESH:D007960] (2662)   Neutrophilia, Hereditary [MESH:C563010] (32)  Leukocytosis [MESH:D007964] (988)  Leukostasis [MESH:D018921] (769)  Eosinophilia [MESH:D004802] (537)   Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134)  Hypereosinophilic Syndrome [MESH:D017681] (119)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Polycythemia [MESH:D011086] (412)   Erythrocytosis, Familial, 4 [MESH:C567086] (86)  Thrombophilia [MESH:D019851] (592)   Antithrombin III Deficiency [MESH:D020152] (80)  Disseminated Intravascular Coagulation [MESH:D004211] (462)  Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Lymphatic Diseases [MESH:D008206] (5167)   Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lymphohistiocytosis, Hemophagocytic [MESH:D051359] (76)   Hemophagocytic lymphohistiocytosis, familial, 2 [MESH:C537250] (38)  Lymphedema [MESH:D008209] (162)   Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 [MESH:C567815] (14)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Sarcoidosis [MESH:D012507] (895)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Leukemia, T-Cell [MESH:D015458] (395)   Leukemia-Lymphoma, Adult T-Cell [MESH:D015459] (138)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Splenic Diseases [MESH:D013158] (1323)   Heterotaxy Syndrome [MESH:D059446] (84)  Hypersplenism [MESH:D006971] (341) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Respiratory System Abnormalities [MESH:D015619] (244)  Situs Inversus [MESH:D012857] (88)  Abnormalities, Multiple [MESH:D000015] (3192)   Hand foot uterus syndrome [MESH:C535627] (20)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Costello Syndrome [MESH:D056685] (407)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Donohue Syndrome [MESH:D056731] (95)  Down Syndrome [MESH:D004314] (1287)  Heterotaxy Syndrome [MESH:D059446] (84)  Incontinentia Pigmenti [MESH:D007184] (57)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Marfan Syndrome [MESH:D008382] (646)  Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Silver-Russell Syndrome [MESH:D056730] (142)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Odontoonychodermal dysplasia [MESH:C537742] (21)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Waardenburg Syndrome [MESH:D014849] (243)   ABCD syndrome [MESH:C535334] (143)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VATER association [MESH:C536534] (46)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Tetralogy of Fallot [MESH:D013771] (121)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 [MESH:C566471] (47)  Heart Septal Defects [MESH:D006343] (385)   Aortopulmonary Septal Defect [MESH:D001028] (47)   Truncus Arteriosus, Persistent [MESH:D014339] (45)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 5 [MESH:C548083] (169)  Vascular Malformations [MESH:D054079] (1108)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1018)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Chromosome Disorders [MESH:D025063] (2030)   Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Down Syndrome [MESH:D004314] (1287)  Silver-Russell Syndrome [MESH:D056730] (142)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)  Anus, Imperforate [MESH:D001006] (140)   VATER association [MESH:C536534] (46)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Arthrogryposis [MESH:D001176] (329)   Distal arthrogryposis type 2B [MESH:C538400] (85)  Lethal Congenital Contracture Syndrome 2 [MESH:C564369] (85)  Craniofacial Abnormalities [MESH:D019465] (3064)   Craniofrontonasal dysplasia [MESH:C536456] (36)  Frontonasal dysplasia [MESH:C538065] (52)  Craniosynostoses [MESH:D003398] (438)  Microcephaly [MESH:D008831] (700)  Craniofacial Dysostosis [MESH:D003394] (391)   Hypertelorism [MESH:D006972] (109)   Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 5 [MESH:C548083] (169)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Chondrodysplasia, acromesomelic, with genital anomalies [MESH:C537913] (20)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Brachydactyly [MESH:D059327] (220)   Brachydactyly type A1 [MESH:C537088] (39)  Brachydactyly type A2 [MESH:C537089] (28)  Brachydactyly, Type D [MESH:C562420] (11)  Acrocapitofemoral Dysplasia [MESH:C564334] (39)  Brachydactyly-Syndactyly Syndrome [MESH:C565193] (11)  Ectromelia [MESH:D004480] (108)   Tetra-amelia autosomal recessive [MESH:C536498] (19)  Foot Deformities, Congenital [MESH:D005532] (538)   Hand foot uterus syndrome [MESH:C535627] (20)  Hand Deformities, Congenital [MESH:D006228] (587)   Hand foot uterus syndrome [MESH:C535627] (20)  Polydactyly [MESH:D017689] (318)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Syndactyly, type v [MESH:C538155] (11)  Brachydactyly-Syndactyly Syndrome [MESH:C565193] (11)  Synpolydactyly 1 [MESH:C566094] (11)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Syndactyly, type v [MESH:C538155] (11)  Brachydactyly-Syndactyly Syndrome [MESH:C565193] (11)  Synpolydactyly 1 [MESH:C566094] (11)  Nervous System Malformations [MESH:D009421] (3354)   Dandy-Walker Syndrome [MESH:D003616] (50)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 2, X-linked [MESH:C536857] (37)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Neuronal Migration Disorders [MESH:D054081] (264)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Encephalocele [MESH:D004677] (151)   Parietal Foramina 2 [MESH:C566510] (9)  Parietal Foramina [MESH:C566826] (42)  Skin Abnormalities [MESH:D012868] (1723)   Incontinentia Pigmenti [MESH:D007184] (57)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Odontoonychodermal dysplasia [MESH:C537742] (21)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Pruriginosa [MESH:C563192] (37)  Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Epidermolysis Bullosa Dystrophica [MESH:D016108] (45)   Epidermolysis bullosa, pretibial [MESH:C535494] (37)  Epidermolysis bullosa dystrophica, Pasini type [MESH:C535956] (37)  Transient bullous dermolysis of the newborn [MESH:C536979] (37)  Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails [MESH:C562638] (37)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Ichthyosis [MESH:D007057] (481)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia [MESH:C565195] (11)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Type IV [MESH:C566293] (8)  Odontodysplasia [MESH:D018126] (24)   Odontoonychodermal dysplasia [MESH:C537742] (21)  Urogenital Abnormalities [MESH:D014564] (2064)   Hand foot uterus syndrome [MESH:C535627] (20)  Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Aromatase deficiency [MESH:C537436] (277)  Hyperandrogenism [MESH:D017588] (98)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Adrenogenital Syndrome [MESH:D047808] (715)   Hyperandrogenism [MESH:D017588] (98)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  Gonadal Dysgenesis [MESH:D006059] (492)   Ovarian Dysgenesis 2 [MESH:C564499] (15)  Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Preaxial deficiency, postaxial polydactyly and hypospadias [MESH:C538278] (20)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Atrial Standstill [MESH:C563984] (32)  Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Cirrhosis, Familial [MESH:C566123] (179)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Costello Syndrome [MESH:D056685] (407)  Cystic Fibrosis [MESH:D003550] (760)  Donohue Syndrome [MESH:D056731] (95)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Marfan Syndrome [MESH:D008382] (646)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 4 [MESH:C567281] (30)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Antithrombin III Deficiency [MESH:D020152] (80)  Thrombasthenia [MESH:D013915] (98)  Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 13 [MESH:C567686] (41)  Chromosome Disorders [MESH:D025063] (2030)   Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Down Syndrome [MESH:D004314] (1287)  Silver-Russell Syndrome [MESH:D056730] (142)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Dwarfism [MESH:D004392] (783)   Silver-Russell Syndrome [MESH:D056730] (142)  Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Retinitis Pigmentosa 7 [MESH:C564284] (8)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Spastic paraplegia 2, X-linked [MESH:C536857] (37)  Panhypopituitarism X-linked [MESH:C538613] (18)  Ovarian Dysgenesis 2 [MESH:C564499] (15)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Atypical Mycobacteriosis, Familial, X-Linked 1 [MESH:C567070] (56)  Mental Retardation, X-Linked, With Panhypopituitarism [MESH:C567485] (18)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (24)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Rett Syndrome [MESH:D015518] (143)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)  Rett Syndrome [MESH:D015518] (143)  Unverricht-Lundborg Syndrome [MESH:D020194] (65)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 2, X-linked [MESH:C536857] (37)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Rett Syndrome [MESH:D015518] (143)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Aromatase deficiency [MESH:C537436] (277)  Xanthinuria, Type I [MESH:C562584] (190)  Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutathione synthetase deficiency [MESH:C536835] (88)  Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis IX [MESH:C562643] (52)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease Type V [MESH:D006012] (165)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Adenylosuccinate lyase deficiency [MESH:C538235] (28)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myasthenic Syndromes, Congenital [MESH:D020294] (155)   Myopathy, Congenital, Compton-North [MESH:C567261] (35)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Wilms Tumor [MESH:D009396] (553)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Skin Diseases, Genetic [MESH:D012873] (3456)   Amyloidosis IX [MESH:C562643] (52)  Erythrokeratodermia Variabilis [MESH:D056266] (26)  Incontinentia Pigmenti [MESH:D007184] (57)  Leukokeratosis, Hereditary Mucosal [MESH:D053529] (51)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Odontoonychodermal dysplasia [MESH:C537742] (21)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (259)   Epidermolysis Bullosa Pruriginosa [MESH:C563192] (37)  Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Epidermolysis Bullosa Dystrophica [MESH:D016108] (45)   Epidermolysis bullosa, pretibial [MESH:C535494] (37)  Epidermolysis bullosa dystrophica, Pasini type [MESH:C535956] (37)  Transient bullous dermolysis of the newborn [MESH:C536979] (37)  Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails [MESH:C562638] (37)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratosis palmoplantaris striata 1 [MESH:C536162] (54)  Keratosis palmoplantaris striata 3 [MESH:C536163] (48)  Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80)   Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)  Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Cystic Fibrosis [MESH:D003550] (760)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Thrombocytopenia, Neonatal Alloimmune [MESH:D054098] (79)  Ichthyosis [MESH:D007057] (476)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)   Spinal muscular atrophy with respiratory distress 1 [MESH:C536880] (15)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Cartilage Diseases [MESH:D002357] (438)  Dermatomyositis [MESH:D003882] (1826)  Marfan Syndrome [MESH:D008382] (646)  Penile Induration [MESH:D010411] (495)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa Dystrophica [MESH:D016108] (45)   Epidermolysis bullosa, pretibial [MESH:C535494] (37)  Epidermolysis bullosa dystrophica, Pasini type [MESH:C535956] (37)  Transient bullous dermolysis of the newborn [MESH:C536979] (37)  Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails [MESH:C562638] (37)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 5 [MESH:C548083] (169)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Exanthema [MESH:D005076] (301)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Pruritus [MESH:D011537] (647)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Skin Neoplasms [MESH:D012878] (2991)  Skin Ulcer [MESH:D012883] (229)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Gynecomastia [MESH:D006177] (484)   Aromatase deficiency [MESH:C537436] (277)  Dermatitis [MESH:D003872] (4530)   Eczema [MESH:D004485] (235)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Seborrheic [MESH:D012628] (58)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Erythrokeratodermia Variabilis [MESH:D056266] (26)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hypotrichosis [MESH:D007039] (1513)   Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Alopecia [MESH:D000505] (1453)   Alopecia Areata [MESH:D000506] (168)  Keratosis [MESH:D007642] (1941)   Erythrokeratodermia Variabilis [MESH:D056266] (26)  Ichthyosis [MESH:D007057] (481)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratosis palmoplantaris striata 1 [MESH:C536162] (54)  Keratosis palmoplantaris striata 3 [MESH:C536163] (48)  Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80)   Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)  Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)  Mastocytosis [MESH:D008415] (60)   Mastocytosis, Cutaneous [MESH:D034701] (45)  Nail Diseases [MESH:D009260] (203)   Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Pigmentation Disorders [MESH:D010859] (1215)   Incontinentia Pigmenti [MESH:D007184] (57)  Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Acanthosis Nigricans [MESH:D000052] (203)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Sebaceous Gland Diseases [MESH:D012625] (245)   Dermatitis, Seborrheic [MESH:D012628] (58)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Skin Abnormalities [MESH:D012868] (1709)   Incontinentia Pigmenti [MESH:D007184] (57)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Odontoonychodermal dysplasia [MESH:C537742] (21)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Pruriginosa [MESH:C563192] (37)  Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Epidermolysis Bullosa Dystrophica [MESH:D016108] (45)   Epidermolysis bullosa, pretibial [MESH:C535494] (37)  Epidermolysis bullosa dystrophica, Pasini type [MESH:C535956] (37)  Transient bullous dermolysis of the newborn [MESH:C536979] (37)  Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails [MESH:C562638] (37)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Ichthyosis [MESH:D007057] (481)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Eczema [MESH:D004485] (235)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Seborrheic [MESH:D012628] (58)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Skin Diseases, Genetic [MESH:D012873] (3481)   Amyloidosis IX [MESH:C562643] (52)  Erythrokeratodermia Variabilis [MESH:D056266] (26)  Incontinentia Pigmenti [MESH:D007184] (57)  Leukokeratosis, Hereditary Mucosal [MESH:D053529] (51)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Odontoonychodermal dysplasia [MESH:C537742] (21)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Pruriginosa [MESH:C563192] (37)  Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Epidermolysis Bullosa Dystrophica [MESH:D016108] (45)   Epidermolysis bullosa, pretibial [MESH:C535494] (37)  Epidermolysis bullosa dystrophica, Pasini type [MESH:C535956] (37)  Transient bullous dermolysis of the newborn [MESH:C536979] (37)  Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails [MESH:C562638] (37)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratosis palmoplantaris striata 1 [MESH:C536162] (54)  Keratosis palmoplantaris striata 3 [MESH:C536163] (48)  Schopf-Schulz-Passarge Syndrome [MESH:C565607] (21)  Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80)   Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)  Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)  Skin Diseases, Infectious [MESH:D012874] (2684)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Viral [MESH:D017193] (203)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Dermatitis, Seborrheic [MESH:D012628] (58)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Urticaria [MESH:D014581] (2668)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Pemphigoid, Bullous [MESH:D010391] (707)  Pemphigus [MESH:D010392] (158)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Pruriginosa [MESH:C563192] (37)  Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Epidermolysis Bullosa Dystrophica [MESH:D016108] (45)   Epidermolysis bullosa, pretibial [MESH:C535494] (37)  Epidermolysis bullosa dystrophica, Pasini type [MESH:C535956] (37)  Transient bullous dermolysis of the newborn [MESH:C536979] (37)  Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails [MESH:C562638] (37)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Metabolic Syndrome X [MESH:D024821] (2151)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)  Calcification of Joints and Arteries [MESH:C565891] (60)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Fanconi Anemia [MESH:D005199] (1604)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes, Gestational [MESH:D016640] (1152)  Donohue Syndrome [MESH:D056731] (95)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 12 [MESH:C563326] (23)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 4 [MESH:C563451] (44)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic Hypoglycemia, Familial, 5 [MESH:C566494] (94)  Insulin Resistance [MESH:D007333] (3511)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   Hyperinsulinemic Hypoglycemia, Familial, 5 [MESH:C566494] (94)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Malabsorption Syndromes [MESH:D008286] (1869)   Diarrhea 5, With Tufting Enteropathy, Congenital [MESH:C567703] (70)  Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Aromatase deficiency [MESH:C537436] (277)  Xanthinuria, Type I [MESH:C562584] (190)  Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutathione synthetase deficiency [MESH:C536835] (88)  Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Hermansky Pudlak syndrome 2 [MESH:C537709] (16)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis IX [MESH:C562643] (52)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease Type V [MESH:D006012] (165)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Adenylosuccinate lyase deficiency [MESH:C538235] (28)  Mitochondrial Diseases [MESH:D028361] (2561)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Meretoja syndrome [MESH:C537459] (95)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis IX [MESH:C562643] (52)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hyponatremia [MESH:D007010] (789)  Water Intoxication [MESH:D014869] (106)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Folic Acid Deficiency [MESH:D005494] (134)  Hyperhomocysteinemia [MESH:D020138] (1716)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Bone Diseases, Endocrine [MESH:D001849] (173)  Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)  Adrenal Insufficiency [MESH:D000309] (1599)   Addison Disease [MESH:D000224] (40)  Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Donohue Syndrome [MESH:D056731] (95)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 12 [MESH:C563326] (23)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 4 [MESH:C563451] (44)  Dwarfism [MESH:D004392] (698)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Gonadal Disorders [MESH:D006058] (5088)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Aromatase deficiency [MESH:C537436] (277)  Hyperandrogenism [MESH:D017588] (98)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Adrenogenital Syndrome [MESH:D047808] (715)   Hyperandrogenism [MESH:D017588] (98)   Mullerian Aplasia and Hyperandrogenism [MESH:C567186] (57)  Gonadal Dysgenesis [MESH:D006059] (492)   Ovarian Dysgenesis 2 [MESH:C564499] (15)  Sexual Infantilism [MESH:D050035] (277)  Hypogonadism [MESH:D007006] (1123)   Sexual Infantilism [MESH:D050035] (277)  Ovarian Diseases [MESH:D010049] (4253)   Chondrodysplasia, acromesomelic, with genital anomalies [MESH:C537913] (20)  Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Hypoparathyroidism [MESH:D007011] (376)   Barakat syndrome [MESH:C537907] (71)  Pituitary Diseases [MESH:D010900] (1829)   Hypopituitarism [MESH:D007018] (732)   Panhypopituitarism X-linked [MESH:C538613] (18)  Mental Retardation, X-Linked, With Panhypopituitarism [MESH:C567485] (18)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)  Hypothyroidism [MESH:D007037] (496)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroiditis [MESH:D013966] (158)   Thyroiditis, Autoimmune [MESH:D013967] (149)   Hashimoto Disease [MESH:D050031] (98) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Addison Disease [MESH:D000224] (40)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Glomerulonephritis, IGA [MESH:D005922] (897)  Graves Disease [MESH:D006111] (278)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Pemphigoid, Bullous [MESH:D010391] (707)  Pemphigus [MESH:D010392] (158)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)   Diabetes Mellitus, Insulin-Dependent, 12 [MESH:C563326] (23)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Urticaria [MESH:D014581] (2668)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Food Hypersensitivity [MESH:D005512] (608)   Peanut Hypersensitivity [MESH:D021183] (572)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (3914)  Immune Complex Diseases [MESH:D007105] (782)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Immunodeficiency without anhidrotic ectodermal dysplasia [MESH:C536289] (56)  WHIM syndrome [MESH:C536697] (148)  Invasive Pneumococcal Disease, Recurrent Isolated, 1 [MESH:C563662] (35)  Invasive Pneumococcal Disease, Recurrent Isolated, 2 [MESH:C564468] (56)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Immunodeficiency due to Defect in CD3-Zeta [MESH:C565712] (19)  MYD88 Deficiency [MESH:C567379] (79)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Lymphopenia [MESH:D008231] (990)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42)  Immunoproliferative Disorders [MESH:D007160] (4761)   Hypergammaglobulinemia [MESH:D006942] (137)  Lymphoproliferative Disorders [MESH:D008232] (4734)   Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 [MESH:C567815] (14)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Leukemia, T-Cell [MESH:D015458] (395)   Leukemia-Lymphoma, Adult T-Cell [MESH:D015459] (138)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765)  Monoclonal Gammopathy of Undetermined Significance [MESH:D008998] (112)   Schnitzler Syndrome [MESH:D019873] (110) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Paratuberculosis [MESH:D010283] (427) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Plaque, Atherosclerotic [MESH:D058226] (696)  Ventricular Remodeling [MESH:D020257] (686)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Gallstones [MESH:D042882] (350)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Hernia [MESH:D006547] (2825)   Encephalocele [MESH:D004677] (151)   Parietal Foramina 2 [MESH:C566510] (9)  Parietal Foramina [MESH:C566826] (42)  Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Diaphragmatic Hernia 3 [MESH:C565710] (22)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Hypertrophy [MESH:D006984] (4476)   Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Prolapse [MESH:D011391] (60)   Pelvic Organ Prolapse [MESH:D056887] (59)  Pathologic Processes [MESH:D010335] (9863)   Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506)  Gliosis [MESH:D005911] (1419)  Hyperbilirubinemia [MESH:D006932] (1860)  Hyperplasia [MESH:D006965] (2463)  Leukocytosis [MESH:D007964] (978)  Muscle Weakness [MESH:D018908] (478)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Sclerosis [MESH:D012598] (224)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial fibrillation, familial 1 [MESH:C538261] (32)  Heart Block [MESH:D006327] (571)   Atrial Standstill [MESH:C563984] (32)  Chromosome Aberrations [MESH:D002869] (2352)   Translocation, Genetic [MESH:D014178] (557)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)  Embryo Loss [MESH:D020964] (288)  Fetal Death [MESH:D005313] (464)  Disease Attributes [MESH:D020969] (3654)   Critical Illness [MESH:D016638] (296)  Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Fibrosis [MESH:D005355] (3133)   Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Granuloma [MESH:D006099] (587)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Growth Disorders [MESH:D006130] (2438)   Acrocapitofemoral Dysplasia [MESH:C564334] (39)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Shock, Hemorrhagic [MESH:D012771] (2042)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Ischemia [MESH:D007511] (3049)   Infarction [MESH:D007238] (298)  No-Reflow Phenomenon [MESH:D054318] (277)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Dysmenorrhea [MESH:D004412] (189)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Necrosis [MESH:D009336] (4019)   Infarction [MESH:D007238] (298)  Osteonecrosis [MESH:D010020] (537)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Asthenia [MESH:D001247] (376)  Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Feminization [MESH:D005262] (655)  Fetal Distress [MESH:D005316] (99)  Flushing [MESH:D005483] (506)  Hypergammaglobulinemia [MESH:D006942] (105)  Reticulocytosis [MESH:D045262] (514)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)   Guanidinoacetate methyltransferase deficiency [MESH:C537622] (60)  Consciousness Disorders [MESH:D003244] (677)   Unconsciousness [MESH:D014474] (657)   Coma [MESH:D003128] (492)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Mental Retardation, X-Linked, With Panhypopituitarism [MESH:C567485] (18)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Spasm [MESH:D013035] (418)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Muscle Spasticity [MESH:D009128] (187)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Pain, Intractable [MESH:D010148] (707)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2298)   Quadriplegia [MESH:D011782] (115)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Reflex, Abnormal [MESH:D012021] (485)   Reflex, Babinski [MESH:D001405] (97)  Sensation Disorders [MESH:D012678] (5009)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness [MESH:D003638] (593)   Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Barakat syndrome [MESH:C537907] (71)  Nephropathy with Pretibial Epidermolysis Bullosa and Deafness [MESH:C563798] (43)  Deafness, Autosomal Recessive 37 [MESH:C564331] (35)  Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia [MESH:C565195] (11)  Deafness, Autosomal Dominant 20 [MESH:C565754] (69)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 2B [MESH:C567214] (18)  Deafness, Autosomal Dominant 2A [MESH:C567441] (36)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Pain [MESH:D010146] (4511)   Arthralgia [MESH:D018771] (191)  Headache [MESH:D006261] (1417)  Pain, Intractable [MESH:D010148] (707)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Pelvic Pain [MESH:D017699] (198)   Dysmenorrhea [MESH:D004412] (189)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Hyperphagia [MESH:D006963] (206)  Nausea [MESH:D009325] (2300)  Diarrhea [MESH:D003967] (858)   Diarrhea, Infantile [MESH:D003968] (72)   Diarrhea 5, With Tufting Enteropathy, Congenital [MESH:C567703] (70)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Cough [MESH:D003371] (179)  Hyperoxia [MESH:D018496] (694)  Hyperventilation [MESH:D006985] (652)  Hypoventilation [MESH:D007040] (359)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Skin Manifestations [MESH:D012877] (1250)   Pruritus [MESH:D011537] (648)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Urological Manifestations [MESH:D020924] (3532)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Foodborne Diseases [MESH:D005517] (269)  Lead Poisoning [MESH:D007855] (515)  Manganese Poisoning [MESH:D020149] (2214)  Mercury Poisoning [MESH:D008630] (193)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Water Intoxication [MESH:D014869] (106)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Phencyclidine Abuse [MESH:D010623] (288)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Tobacco Use Disorder [MESH:D014029] (628)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Morphine Dependence [MESH:D009021] (855) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Fractures, Bone [MESH:D050723] (597)   Hip Fractures [MESH:D006620] (81)  Femoral Fractures [MESH:D005264] (137)   Hip Fractures [MESH:D006620] (82)  Hip Injuries [MESH:D025981] (83)   Hip Fractures [MESH:D006620] (81)  Leg Injuries [MESH:D007869] (152)   Femoral Fractures [MESH:D005264] (137)   Hip Fractures [MESH:D006620] (82)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D23. Biological Factors  D23. Biological Factors  Biological Factors [MESH:D001685] (12003)   Toxins, Biological [MESH:D014118] (2185) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Physical Examination [MESH:D010808] (1041)   Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Mental Retardation, X-Linked, With Panhypopituitarism [MESH:C567485] (18)  Mental Disorders [MESH:D001523] (2063)   Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Dementia [MESH:D003704] (471)   Alzheimer Disease [MESH:D000544] (242)   Alzheimer disease type 2 [MESH:C536595] (165)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Mental Retardation, X-Linked, With Panhypopituitarism [MESH:C567485] (18)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XX Disorders of Sex Development [MESH:D058489] (375)   Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (388)   Persistent Mullerian duct syndrome [MESH:C536665] (47) G. Phenomena and Processes  G. Phenomena and Processes  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Physiological Phenomena [MESH:D010829] (788)   Pharmacological Phenomena [MESH:D002620] (173)   Drug Resistance [MESH:D004351] (139)   Insulin Resistance [MESH:D007333] (97)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)