Item 37 of 642 (back to results) previous next   retinol acetate C009166               MeSH Unique Identifier: C009166 Chemical – Gene Interaction Note 1: Retinol acetate binds to ALB protein Click here for more information

Current search: C12. Male Urogenital Diseases: Male Urogenital Diseases [MESH:D052801] > Urologic Diseases [MESH:D014570] > Kidney Diseases [MESH:D007674] > Nephritis [MESH:D009393] > Glomerulonephritis [MESH:D005921] > Glomerulonephritis, Membranous [MESH:D015433] × Select any link to see items in a related category. more general categories    information about this item 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423) 4. Semantic Terms  4. Semantic Terms  Entity [STY:T071] (48056)   Physical Object [STY:T072] (47583)   Substance [STY:T167] (46174)   Chemical [STY:T103] (46110)   Chemical Viewed Functionally [STY:T120] (28747)   Pharmacologic Substance [STY:T121] (11019)  Biologically Active Substance [STY:T123] (16941)   Vitamin [STY:T127] (70)  Chemical Viewed Structurally [STY:T104] (44741)   Organic Chemical [STY:T109] (44144) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Head [MESH:D006257] (523)   Face [MESH:D005145] (387)   Eye [MESH:D005123] (148)   Eyelids [MESH:D005143] (143)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Hypochondroplasia [MESH:C562937] (66)  Skull [MESH:D012886] (610)   Thanatophoric dysplasia, type 2 [MESH:C536508] (66)  Sense Organs [MESH:D012679] (1060)   Eye [MESH:D005123] (858)   Eyelids [MESH:D005143] (146)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Tissues [MESH:D014024] (397)   Connective Tissue [MESH:D003238] (173)   Bone and Bones [MESH:D001842] (149)   Hypochondroplasia [MESH:C562937] (66) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Tuberculosis [MESH:D014376] (992)   Tuberculosis, Bovine [MESH:D014380] (380) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Herpesviridae Infections [MESH:D006566] (1944)   Sarcoma, Kaposi [MESH:D012514] (1578)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  RNA Virus Infections [MESH:D012327] (4215)   Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   HIV Seropositivity [MESH:D006679] (480)  HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   HIV Seropositivity [MESH:D006679] (480)  HIV Wasting Syndrome [MESH:D019247] (1956)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  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)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Precancerous Conditions [MESH:D011230] (2858)  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)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  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, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Kaposi [MESH:D012514] (1578)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Germinoma [MESH:D018237] (201)   Seminoma [MESH:D018239] (195)  Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   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)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (169)  Prolactinoma [MESH:D015175] (312)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Squamous Cell [MESH:D002294] (4294)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   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)   Carcinoma, Squamous Cell [MESH:D002294] (4294)  Papilloma [MESH:D010212] (2243)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   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)  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)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Nevus [MESH:D009506] (340)   Nevus, Pigmented [MESH:D009508] (123)   Nevus, Epidermal [MESH:C562736] (112)  Neoplasms by Site [MESH:D009371] (9169)   Breast Neoplasms [MESH:D001943] (6077)  Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Digestive System Neoplasms [MESH:D004067] (7487)   Gastrointestinal Neoplasms [MESH:D005770] (6452)   Esophageal Neoplasms [MESH:D004938] (3737)  Stomach Neoplasms [MESH:D013274] (4942)  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)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Prolactinoma [MESH:D015175] (312)  Head and Neck Neoplasms [MESH:D006258] (4612)   Esophageal Neoplasms [MESH:D004938] (3737)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  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)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Skin Neoplasms [MESH:D012878] (2992)   Nevus, Epidermal [MESH:C562736] (112)  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)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  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 Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Osteitis Deformans [MESH:D010001] (287)  Osteonecrosis [MESH:D010020] (539)  Bone Diseases, Developmental [MESH:D001848] (3315)   CATSHL syndrome [MESH:C537975] (66)  Marfan Syndrome [MESH:D008382] (646)  Acro-Osteolysis [MESH:D030981] (548)   Hajdu-Cheney Syndrome [MESH:D031845] (42)  Dwarfism [MESH:D004392] (778)   Hypochondroplasia [MESH:C562937] (66)  Achondroplasia [MESH:D000130] (196)   Thanatophoric Dysplasia [MESH:D013796] (147)   Thanatophoric dysplasia, type 1 [MESH:C536507] (66)  Thanatophoric dysplasia, type 2 [MESH:C536508] (66)  Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)   Crouzon Syndrome With Acanthosis Nigricans [MESH:C567382] (66)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Muenke Syndrome [MESH:C537369] (66)  Craniosynostosis, Type 2 [MESH:C565753] (36)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Osteochondrodysplasias [MESH:D010009] (2440)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Achondroplasia [MESH:D000130] (196)   Thanatophoric Dysplasia [MESH:D013796] (147)   Thanatophoric dysplasia, type 1 [MESH:C536507] (66)  Thanatophoric dysplasia, type 2 [MESH:C536508] (66)  Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)   Tumoral Calcinosis, Hyperphosphatemic, Familial [MESH:C566870] (94)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  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)   Hajdu-Cheney Syndrome [MESH:D031845] (42)  Hyperostosis [MESH:D015576] (493)   Exostoses [MESH:D005096] (160)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)   Tumoral Calcinosis, Hyperphosphatemic, Familial [MESH:C566870] (94)  Spinal Diseases [MESH:D013122] (2485)   Spinal Curvatures [MESH:D013121] (742)   Scoliosis [MESH:D012600] (194)  Lordosis [MESH:D008141] (69)   Hypochondroplasia [MESH:C562937] (66)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   CATSHL syndrome [MESH:C537975] (66)  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)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Muscular Diseases [MESH:D009135] (4071)   Mitochondrial Myopathies [MESH:D017240] (2176)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2071)   Polymyositis [MESH:D017285] (2007)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Craniofacial Dysostosis [MESH:D003394] (391)   Crouzon Syndrome With Acanthosis Nigricans [MESH:C567382] (66)  Craniosynostoses [MESH:D003398] (438)   Muenke Syndrome [MESH:C537369] (66)  Craniosynostosis, Type 2 [MESH:C565753] (36)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Microcephaly [MESH:D008831] (700)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Muenke Syndrome [MESH:C537369] (66)  Craniosynostosis, Type 2 [MESH:C565753] (36)  Limb Deformities, Congenital [MESH:D017880] (1813)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Hypochondroplasia [MESH:C562937] (66)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Thanatophoric Dysplasia [MESH:D013796] (147)   Thanatophoric dysplasia, type 1 [MESH:C536507] (66)  Thanatophoric dysplasia, type 2 [MESH:C536508] (66)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   CATSHL syndrome [MESH:C537975] (66)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Muenke Syndrome [MESH:C537369] (66)  Craniosynostosis, Type 2 [MESH:C565753] (36)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  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)   Alagille Syndrome [MESH:D016738] (105)  Digestive System Fistula [MESH:D016154] (102)   Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Digestive System Neoplasms [MESH:D004067] (7493)   Gastrointestinal Neoplasms [MESH:D005770] (6460)   Esophageal Neoplasms [MESH:D004938] (3737)  Stomach Neoplasms [MESH:D013274] (4942)  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)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Esophageal Neoplasms [MESH:D004938] (3737)  Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Gastroenteritis [MESH:D005759] (4066)   Colitis [MESH:D003092] (3199)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Esophageal Neoplasms [MESH:D004938] (3737)  Stomach Neoplasms [MESH:D013274] (4942)  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)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   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)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Budd-Chiari Syndrome [MESH:D006502] (164)  Hepatolenticular Degeneration [MESH:D006527] (473)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Alagille Syndrome [MESH:D016738] (105)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) 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)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Mouth Diseases [MESH:D009059] (4783)   Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Pharyngeal Diseases [MESH:D010608] (1562)   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)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Anodontia [MESH:D000848] (185)   Witkop syndrome [MESH:C536736] (38)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Type IV [MESH:C566293] (8)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Anodontia [MESH:D000848] (185)   Witkop syndrome [MESH:C536736] (38)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Type IV [MESH:C566293] (8) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Lung Diseases [MESH:D008171] (7249)   Pneumonia [MESH:D011014] (3482)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Berylliosis [MESH:D001607] (2005)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Lung Injury [MESH:D055370] (3688)   Pneumoconiosis [MESH:D011009] (2789)   Berylliosis [MESH:D001607] (2005)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Paranasal Sinus Diseases [MESH:D010254] (476)   Sinusitis [MESH:D012852] (469)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Respiratory Tract Fistula [MESH:D016156] (91)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Respiratory Tract Infections [MESH:D012141] (3926)   Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Sinusitis [MESH:D012852] (469)  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)  Tracheal Diseases [MESH:D014133] (107)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58) 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)   CATSHL syndrome [MESH:C537975] (66)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Paranasal Sinus Diseases [MESH:D010254] (476)   Sinusitis [MESH:D012852] (469)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)  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)   Neurotoxicity Syndromes [MESH:D020258] (4570)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   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 Injuries [MESH:D001930] (3429)  Brain Neoplasms [MESH:D001932] (2764)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Cerebellar Diseases [MESH:D002526] (736)   Spinocerebellar Degenerations [MESH:D013132] (449)   Friedreich Ataxia [MESH:D005621] (34)  Cerebrovascular Disorders [MESH:D002561] (5542)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  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)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  Alzheimer disease type 4 [MESH:C536596] (42)  Epilepsy [MESH:D004827] (6274)   Status Epilepticus [MESH:D013226] (4014)  Seizures [MESH:D012640] (4502)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Prolactinoma [MESH:D015175] (312)  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)   Hepatolenticular Degeneration [MESH:D006527] (473)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Spinal Cord Diseases [MESH:D013118] (4376)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal muscular atrophy 4 [MESH:C538417] (31)  Spinal Muscular Atrophies of Childhood [MESH:D014897] (55)  Spinocerebellar Degenerations [MESH:D013132] (449)   Friedreich Ataxia [MESH:D005621] (34)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Nervous System Malformations [MESH:D009421] (3354)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Acrocallosal Syndrome [MESH:D055673] (43)  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, Axonal, Type 2a1 [MESH:C566138] (54)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Nervous System Neoplasms [MESH:D009423] (3073)   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)   von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hepatolenticular Degeneration [MESH:D006527] (473)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Spinal Muscular Atrophies of Childhood [MESH:D014897] (55)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Spinocerebellar Degenerations [MESH:D013132] (449)   Friedreich Ataxia [MESH:D005621] (34)  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 4 [MESH:C538417] (31)  Spinal Muscular Atrophies of Childhood [MESH:D014897] (55)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  Alzheimer disease type 4 [MESH:C536596] (42)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neurologic Manifestations [MESH:D009461] (8964)   Neurobehavioral Manifestations [MESH:D019954] (5230)   Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Seizures [MESH:D012640] (4514)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   CATSHL syndrome [MESH:C537975] (66)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  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 4 [MESH:C538417] (31)  Spinal Muscular Atrophies of Childhood [MESH:D014897] (55)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Spinal muscular atrophy 4 [MESH:C538417] (31)  Spinal Muscular Atrophies of Childhood [MESH:D014897] (55)  Muscular Diseases [MESH:D009135] (3538)   Mitochondrial Myopathies [MESH:D017240] (2176)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2069)   Polymyositis [MESH:D017285] (2007)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Mononeuropathies [MESH:D020422] (604)   Sciatic Neuropathy [MESH:D020426] (477)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Corneal Diseases [MESH:D003316] (1445)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Eye Abnormalities [MESH:D005124] (1233)   Microphthalmos [MESH:D008850] (273)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Retinal Diseases [MESH:D012164] (3747)   Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Fundus Dystrophy, Pseudoinflammatory, Of Sorsby [MESH:C564992] (121)  Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Infertility [MESH:D007246] (2909)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)  Urogenital Abnormalities [MESH:D014564] (2065)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Cryptorchidism [MESH:D003456] (215)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Lipoprotein Glomerulopathy [MESH:C567089] (165)  Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Lupus Nephritis [MESH:D008181] (602)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) 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)  Infertility [MESH:D007246] (2211)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Uterine Diseases [MESH:D014591] (2479)   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)  Urogenital Abnormalities [MESH:D014564] (2043)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Lipoprotein Glomerulopathy [MESH:C567089] (165)  Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Lupus Nephritis [MESH:D008181] (602)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316) 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)   Alagille Syndrome [MESH:D016738] (105)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  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 Failure [MESH:D006333] (4058)  Heart Valve Diseases [MESH:D006349] (3333)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1V [MESH:C566856] (42)  Cardiomyopathies [MESH:D009202] (5331)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1V [MESH:C566856] (42)  Heart Defects, Congenital [MESH:D006330] (2443)   Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Angioedema [MESH:D000799] (837)  Diabetic Angiopathies [MESH:D003925] (1984)  Hypertension [MESH:D006973] (5655)  Hypotension [MESH:D007022] (4045)  Vasculitis [MESH:D014657] (2604)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  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)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebral Arterial Diseases [MESH:D002539] (2440)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Embolism and Thrombosis [MESH:D016769] (3374)   Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)   Budd-Chiari Syndrome [MESH:D006502] (164)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Telangiectasis [MESH:D013684] (255)   Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Anemia [MESH:D000740] (3966)   Anemia, Hemolytic [MESH:D000743] (3083)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Blood Protein Disorders [MESH:D001796] (3051)   Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Hemorrhagic Disorders [MESH:D006474] (3359)   Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)  Leukocyte Disorders [MESH:D007960] (2662)   Eosinophilia [MESH:D004802] (537)  Lymphatic Diseases [MESH:D008206] (5167)   Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   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, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Splenic Diseases [MESH:D013158] (1323)   Heterotaxy Syndrome [MESH:D059446] (84) 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)   Situs Inversus [MESH:D012857] (88)  Abnormalities, Multiple [MESH:D000015] (3192)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Alagille Syndrome [MESH:D016738] (105)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Wolf-Hirschhorn Syndrome [MESH:D054877] (72)  Ectodermal Dysplasia [MESH:D004476] (938)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Waardenburg Syndrome [MESH:D014849] (243)   Waardenburg Syndrome, Type 2D [MESH:C563839] (48)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Alagille Syndrome [MESH:D016738] (105)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Vascular Malformations [MESH:D054079] (1108)   Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)  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)  Chromosome Disorders [MESH:D025063] (2030)   Wolf-Hirschhorn Syndrome [MESH:D054877] (72)  Eye Abnormalities [MESH:D005124] (1233)   Microphthalmos [MESH:D008850] (273)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Hajdu-Cheney Syndrome [MESH:D031845] (42)  Craniofacial Abnormalities [MESH:D019465] (3064)   Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Craniofacial Dysostosis [MESH:D003394] (391)   Crouzon Syndrome With Acanthosis Nigricans [MESH:C567382] (66)  Craniosynostoses [MESH:D003398] (438)   Muenke Syndrome [MESH:C537369] (66)  Craniosynostosis, Type 2 [MESH:C565753] (36)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Microcephaly [MESH:D008831] (700)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Muenke Syndrome [MESH:C537369] (66)  Craniosynostosis, Type 2 [MESH:C565753] (36)  Limb Deformities, Congenital [MESH:D017880] (1813)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Hypochondroplasia [MESH:C562937] (66)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Hand Deformities, Congenital [MESH:D006228] (587)   CATSHL syndrome [MESH:C537975] (66)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Thanatophoric Dysplasia [MESH:D013796] (147)   Thanatophoric dysplasia, type 1 [MESH:C536507] (66)  Thanatophoric dysplasia, type 2 [MESH:C536508] (66)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Muenke Syndrome [MESH:C537369] (66)  Craniosynostosis, Type 2 [MESH:C565753] (36)  Syndactyly [MESH:D013576] (487)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Nervous System Malformations [MESH:D009421] (3354)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Acrocallosal Syndrome [MESH:D055673] (43)  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, Axonal, Type 2a1 [MESH:C566138] (54)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Skin Abnormalities [MESH:D012868] (1723)   Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 11 [MESH:C567410] (101)  Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Anodontia [MESH:D000848] (185)   Witkop syndrome [MESH:C536736] (38)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Type IV [MESH:C566293] (8)  Urogenital Abnormalities [MESH:D014564] (2064)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Cryptorchidism [MESH:D003456] (215)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Alagille Syndrome [MESH:D016738] (105)  Hajdu-Cheney Syndrome [MESH:D031845] (42)  Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478)  Marfan Syndrome [MESH:D008382] (646)  Chromosome Disorders [MESH:D025063] (2030)   Wolf-Hirschhorn Syndrome [MESH:D054877] (72)  Dwarfism [MESH:D004392] (783)   Hypochondroplasia [MESH:C562937] (66)  Achondroplasia [MESH:D000130] (196)   Thanatophoric Dysplasia [MESH:D013796] (147)   Thanatophoric dysplasia, type 1 [MESH:C536507] (66)  Thanatophoric dysplasia, type 2 [MESH:C536508] (66)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Mental Retardation, X-Linked [MESH:D038901] (1867)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hepatolenticular Degeneration [MESH:D006527] (473)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Spinal Muscular Atrophies of Childhood [MESH:D014897] (55)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Spinocerebellar Degenerations [MESH:D013132] (449)   Friedreich Ataxia [MESH:D005621] (34)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)   Tumoral Calcinosis, Hyperphosphatemic, Familial [MESH:C566870] (94)  Thanatophoric Dysplasia [MESH:D013796] (147)   Thanatophoric dysplasia, type 1 [MESH:C536507] (66)  Thanatophoric dysplasia, type 2 [MESH:C536508] (66) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Marfan Syndrome [MESH:D008382] (646)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Drug Eruptions [MESH:D003875] (2697)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   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)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Acanthosis Nigricans [MESH:D000052] (203)   Crouzon Syndrome With Acanthosis Nigricans [MESH:C567382] (66)  Hypopigmentation [MESH:D017496] (718)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Skin Abnormalities [MESH:D012868] (1709)   Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Dermatitis, Atopic [MESH:D003876] (2052)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Skin Neoplasms [MESH:D012878] (2991)   Nevus, Epidermal [MESH:C562736] (112) 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)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Tumoral Calcinosis, Hyperphosphatemic, Familial [MESH:C566870] (94)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  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)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  Mitochondrial Diseases [MESH:D028361] (2561)   Friedreich Ataxia [MESH:D005621] (34)  Mitochondrial Myopathies [MESH:D017240] (2176)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hyperphosphatemia [MESH:D054559] (159)   Tumoral Calcinosis, Hyperphosphatemic, Familial [MESH:C566870] (94)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)  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)   Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Angiopathies [MESH:D003925] (1984)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Dwarfism [MESH:D004392] (698)   Hypochondroplasia [MESH:C562937] (66)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Prolactinoma [MESH:D015175] (312)  Gonadal Disorders [MESH:D006058] (5088)   Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Cryptorchidism [MESH:D003456] (215)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Prolactinoma [MESH:D015175] (312)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroxinemia [MESH:D006981] (659)   Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Immune Complex Diseases [MESH:D007105] (782)   Serum Sickness [MESH:D012713] (484)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  HIV Infections [MESH:D015658] (3402)   HIV Seropositivity [MESH:D006679] (480)  HIV Wasting Syndrome [MESH:D019247] (1956)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   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)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   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, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Cattle Diseases [MESH:D002418] (416)   Tuberculosis, Bovine [MESH:D014380] (380) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Plaque, Atherosclerotic [MESH:D058226] (696)  Fistula [MESH:D005402] (130)   Digestive System Fistula [MESH:D016154] (102)   Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Hypertrophy [MESH:D006984] (4476)   Splenomegaly [MESH:D013163] (1258)  Nails, Malformed [MESH:D009264] (184)   Witkop syndrome [MESH:C536736] (38)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Emphysema [MESH:D004646] (1096)  Hyperplasia [MESH:D006965] (2463)  Inflammation [MESH:D007249] (5241)  Ischemia [MESH:D007511] (3049)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Necrosis [MESH:D009336] (4019)   Osteonecrosis [MESH:D010020] (537)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Shock, Hemorrhagic [MESH:D012771] (2042)  Signs and Symptoms [MESH:D012816] (10659)   Aging, Premature [MESH:D019588] (66)  Edema [MESH:D004487] (3726)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  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)  Neurologic Manifestations [MESH:D009461] (8702)   Neurobehavioral Manifestations [MESH:D019954] (4706)   Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Seizures [MESH:D012640] (4502)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   CATSHL syndrome [MESH:C537975] (66)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Respiratory Sounds [MESH:D012135] (713)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005) 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)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Mercury Poisoning [MESH:D008630] (193)  Neurotoxicity Syndromes [MESH:D020258] (3323)  Substance-Related Disorders [MESH:D019966] (6308)   Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Phencyclidine Abuse [MESH:D010623] (288)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) 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)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Fractures, Bone [MESH:D050723] (597)   Femoral Fractures [MESH:D005264] (137)  Leg Injuries [MESH:D007869] (152)   Femoral Fractures [MESH:D005264] (137)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  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) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Acyclic [MESH:D006839] (3563)   Alkenes [MESH:D000475] (2079)   Polyenes [MESH:D011090] (1230)   Carotenoids [MESH:D002338] (585)   Retinoids [MESH:D012176] (281)   Vitamin A [MESH:D014801] (141)  Hydrocarbons, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Alicyclic [MESH:D006840] (3199)   Cycloparaffins [MESH:D003516] (3197)   Cyclohexanes [MESH:D003510] (1589)   Cyclohexenes [MESH:D053138] (756)   Carotenoids [MESH:D002338] (579)   Retinoids [MESH:D012176] (275)   Vitamin A [MESH:D014801] (141)  Terpenes [MESH:D013729] (10347)   Carotenoids [MESH:D002338] (585)   Retinoids [MESH:D012176] (281)   Vitamin A [MESH:D014801] (141) D23. Biological Factors  D23. Biological Factors  Biological Factors [MESH:D001685] (12003)   Pigments, Biological [MESH:D010860] (2018)   Carotenoids [MESH:D002338] (508)   Retinoids [MESH:D012176] (281)   Vitamin A [MESH:D014801] (58) 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)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Psychomotor Disorders [MESH:D011596] (250)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  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)  Alzheimer disease type 4 [MESH:C536596] (42)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)