Item 18 of 111 (back to results) previous next   3,4,3',4'-tetrachlorobiphenyl C028451               MeSH Unique Identifier: C028451 Chemical – Gene Interaction Note 1: 3,4,3',4'-tetrachlorobiphenyl binds to AHR protein Note 2: 3,4,3',4'-tetrachlorobiphenyl binds to and results in increased activity of AHR protein Click here for more information

Current search: C20. Immune System Diseases: Immune System Diseases [MESH:D007154] > Hypersensitivity [MESH:D006967] > Hypersensitivity, Immediate [MESH:D006969] > Urticaria [MESH:D014581] > Angioedema [MESH:D000799] > Angioedemas, Hereditary [MESH:D054179] > Hereditary Angioedema Types I and II [MESH:D056829] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  A-kinase anchor proteins [HGNC:AKAP] (99)   A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)  CD molecules [HGNC:CD] (1459)   chemokine (C-C motif) receptor 01 [HGNC:CCR1] (21)  Chemokine receptors [HGNC:CR] (207)   Chemokine (C-C motif) receptors [HGNC:CCR] (92)   chemokine (C-C motif) receptor 01 [HGNC:CCR1] (21)  Collagens [HGNC:COL] (230)   collagen, type III, alpha 1 [HGNC:COL3A1] (33)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566)  cytochrome P450, family 11, subfamily B, polypeptide 01 [HGNC:CYP11B1] (41)  cytochrome P450, family 11, subfamily B, polypeptide 02 [HGNC:CYP11B2] (71)  Intraflagellar transport homologs [HGNC:IFT] (19)   intraflagellar transport 088 homolog (Chlamydomonas) [HGNC:IFT88] (10)  Nuclear hormone receptors [HGNC:NR] (1322)   estrogen receptor 1 [HGNC:ESR1] (506)  Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227)   A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)  son of sevenless homolog 1 (Drosophila) [HGNC:SOS1] (27)  Rho guanine nucleotide exchange factors [HGNC:ARHGEF] (105)   A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)  son of sevenless homolog 1 (Drosophila) [HGNC:SOS1] (27)  L ribosomal proteins [HGNC:RPL] (79)   ribosomal protein L35a [HGNC:RPL35A] (7)  SH2 domain containing [HGNC:SH2D] (431)   spleen tyrosine kinase [HGNC:SYK] (11)  Solute carriers [HGNC:SLC] (716)   solute carrier family 07 (anionic amino acid transporter light chain, xc- system), member 11 [HGNC:SLC7A11] (77)  Tetratricopeptide repeat domain containing [HGNC:TTC] (153)   intraflagellar transport 088 homolog (Chlamydomonas) [HGNC:IFT88] (10)  ZINC FINGERS [HGNC:ZNF] (383)   Zinc fingers, C2H2-type [HGNC:ZNF] (349)   GLI family zinc finger 2 [HGNC:GLI2] (15) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  cotreatment (1499)  expression (494)  Decreases (5154)   abundance (224)  reaction (3393)  Increases (5571)   activity (2865)  expression (3238)  reaction (1574) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Holoprosencephaly 9 [MESH:C563659] (35)  Head [MESH:D006257] (523)   Face [MESH:D005145] (387)   Coffin-Siris syndrome [MESH:C536436] (102)  Neck [MESH:D009333] (107)   Coffin-Siris syndrome [MESH:C536436] (102)  Musculoskeletal System [MESH:D009141] (1255)   Muscles [MESH:D009132] (97)   Muscle, Skeletal [MESH:D018482] (86)   Abdominal Muscles [MESH:D000009] (49)   Carnevale syndrome [MESH:C535586] (45)  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)  Endocrine System [MESH:D004703] (206)   Endocrine Glands [MESH:D004702] (193)   Pituitary Gland [MESH:D010902] (45)   Pituitary Gland, Anterior [MESH:D010903] (41)   Holoprosencephaly 9 [MESH:C563659] (35)  Neurosecretory Systems [MESH:D009490] (49)   Hypothalamo-Hypophyseal System [MESH:D007030] (47)   Pituitary Gland [MESH:D010902] (45)   Pituitary Gland, Anterior [MESH:D010903] (41)   Holoprosencephaly 9 [MESH:C563659] (35)  Nervous System [MESH:D009420] (587)   Central Nervous System [MESH:D002490] (371)   Brain [MESH:D001921] (349)   Prosencephalon [MESH:D016548] (154)   Diencephalon [MESH:D004027] (80)   Hypothalamus [MESH:D007031] (62)   Hypothalamus, Middle [MESH:D007033] (52)   Hypothalamo-Hypophyseal System [MESH:D007030] (47)   Pituitary Gland [MESH:D010902] (45)   Pituitary Gland, Anterior [MESH:D010903] (41)   Holoprosencephaly 9 [MESH:C563659] (35)  Neurosecretory Systems [MESH:D009490] (52)   Hypothalamo-Hypophyseal System [MESH:D007030] (47)   Pituitary Gland [MESH:D010902] (45)   Pituitary Gland, Anterior [MESH:D010903] (41)   Holoprosencephaly 9 [MESH:C563659] (35)  Sense Organs [MESH:D012679] (1060)   Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Peters anomaly [MESH:C537884] (465) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Neisseriaceae Infections [MESH:D016870] (273)  Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)  Tuberculosis [MESH:D014376] (992)   Tuberculosis, Pulmonary [MESH:D014397] (678)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Skin Diseases, Bacterial [MESH:D017192] (157)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  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)   Skin Diseases, Bacterial [MESH:D017192] (156)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Suppuration [MESH:D013492] (219)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) 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)   Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Enterovirus Infections [MESH:D004769] (241)   Coxsackievirus Infections [MESH:D003384] (194)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   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 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)   Hamartoma [MESH:D006222] (1484)  Cysts [MESH:D003560] (2625)   Bone Cysts [MESH:D001845] (78)   Jaw Cysts [MESH:D007570] (74)   Odontogenic Cysts [MESH:D009807] (72)   Basal Cell Nevus Syndrome [MESH:D001478] (67)  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)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   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)  Smooth Muscle Tumor [MESH:D018235] (132)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Leiomyosarcoma [MESH:D007890] (977)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Kaposi [MESH:D012514] (1578)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   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)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   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)  Thyroid cancer, papillary [MESH:C536915] (111)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  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, Basal Cell [MESH:D002280] (1628)   Basal Cell Nevus Syndrome [MESH:D001478] (67)  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)   Basal Cell Nevus Syndrome [MESH:D001478] (67)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  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)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  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)   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)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Sarcoma, Kaposi [MESH:D012514] (1578)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioma, capillary infantile [MESH:C535860] (190)  Hemangioblastoma [MESH:D018325] (395)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  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)   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)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  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)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  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)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   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)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  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)  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)   Anaplasia [MESH:D000708] (348)  Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  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)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Basal Cell Nevus Syndrome [MESH:D001478] (67)  Precancerous Conditions [MESH:D011230] (2858)   Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  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)   Bone Neoplasms [MESH:D001859] (1334)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromesomelic dysplasia, Maroteaux type [MESH:C535661] (29)  Basal Cell Nevus Syndrome [MESH:D001478] (67)  Osteochondrodysplasias [MESH:D010009] (2440)  Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)  Spinal Diseases [MESH:D013122] (2485)   Spinal Curvatures [MESH:D013121] (742)   Kyphosis [MESH:D007738] (637)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Jaw Cysts [MESH:D007570] (74)   Odontogenic Cysts [MESH:D009807] (72)   Basal Cell Nevus Syndrome [MESH:D001478] (67)  Joint Diseases [MESH:D007592] (4657)   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)  Gout [MESH:D006073] (261)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Systemic carnitine deficiency [MESH:C536778] (92)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  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 Dystrophies, Limb-Girdle [MESH:D049288] (259)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Distal Myopathies [MESH:D049310] (178)   Distal myopathy, Nonaka type [MESH:C536816] (40)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Myositis, Inclusion Body [MESH:D018979] (103)   Inclusion body myopathy autosomal recessive [MESH:C538329] (40)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Costello Syndrome [MESH:D056685] (407)  Donohue Syndrome [MESH:D056731] (95)  Microcephaly [MESH:D008831] (700)  Silver-Russell Syndrome [MESH:D056730] (142)  Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 9 [MESH:C563659] (35)  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)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  Noonan Syndrome 5 [MESH:C548083] (169)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Hip Dislocation, Congenital [MESH:D006618] (56)   Carnevale syndrome [MESH:C535586] (45)  Limb Deformities, Congenital [MESH:D017880] (1813)   Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Polydactyly [MESH:D017689] (318)   Holoprosencephaly 9 [MESH:C563659] (35)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Gout [MESH:D006073] (261)  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)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Digestive System Neoplasms [MESH:D004067] (7493)   Gastrointestinal Neoplasms [MESH:D005770] (6460)   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)   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)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  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)  Gastroenteritis [MESH:D005759] (4066)   Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 10 [MESH:C567021] (18)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   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)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Intestinal Perforation [MESH:D007416] (471)  Mesenteric Vascular Occlusion [MESH:D008641] (147)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 10 [MESH:C567021] (18)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   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)  Malabsorption Syndromes [MESH:D008286] (492)   Celiac Disease [MESH:D002446] (340)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  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)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Budd-Chiari Syndrome [MESH:D006502] (164)  Hepatomegaly [MESH:D006529] (1169)  Hypertension, Portal [MESH:D006975] (869)  Zellweger Syndrome [MESH:D015211] (182)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Fatty Liver, Alcoholic [MESH:D005235] (657)  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)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Protoporphyria, Erythropoietic [MESH:D046351] (49)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Peritoneal Diseases [MESH:D010532] (1119)   Mesenteric Vascular Occlusion [MESH:D008641] (147) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Jaw Cysts [MESH:D007570] (74)   Odontogenic Cysts [MESH:D009807] (72)   Basal Cell Nevus Syndrome [MESH:D001478] (67)  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)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330) 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)   Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Lung Diseases [MESH:D008171] (7249)   Hypertension, Pulmonary [MESH:D006976] (2000)  Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Fibrosis [MESH:D011658] (3140)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  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)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Hyperventilation [MESH:D006985] (654)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   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)   Deafness [MESH:D003638] (623)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Central Nervous System Diseases [MESH:D002493] (9745)   Meningitis [MESH:D008581] (352)  Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia musculorum deformans type 1 [MESH:C538005] (21)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Phenylketonurias [MESH:D010661] (156)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Peroxisomal Disorders [MESH:D018901] (1472)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease, Infantile [MESH:D052919] (51)  Zellweger Syndrome [MESH:D015211] (182)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Citrullinemia [MESH:D020159] (99)   Neonatal-onset citrullinemia type 2 [MESH:C536398] (35)  Adult-onset citrullinemia type 2 [MESH:C538053] (35)  Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Ataxia Telangiectasia [MESH:D001260] (142)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 28 [MESH:C537205] (13)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Cerebrovascular Disorders [MESH:D002561] (5542)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Artery Thrombosis [MESH:D002341] (138)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)  Lewy Body Disease [MESH:D020961] (1143)  Epilepsy [MESH:D004827] (6274)   Amish Infantile Epilepsy Syndrome [MESH:C563799] (46)  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)  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)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1250)   Hyperprolactinemia [MESH:D006966] (603)  Hypopituitarism [MESH:D007018] (732)   Holoprosencephaly 9 [MESH:C563659] (35)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  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)   Dyskinesias [MESH:D020820] (1827)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Dystonic Disorders [MESH:D020821] (729)   Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia musculorum deformans type 1 [MESH:C538005] (21)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  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)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 28 [MESH:C537205] (13)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Chronobiology Disorders [MESH:D021081] (970)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (93)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Strabismus [MESH:D013285] (79)   Carnevale syndrome [MESH:C535586] (45)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Corpus callosum agenesis neuronopathy [MESH:C536446] (20)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 9 [MESH:C563659] (35)  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 4B2 [MESH:C535421] (10)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Ataxia Telangiectasia [MESH:D001260] (142)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia musculorum deformans type 1 [MESH:C538005] (21)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4B2 [MESH:C535421] (10)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 28 [MESH:C537205] (13)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  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)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Frontotemporal Lobar Degeneration [MESH:D057174] (308)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Ataxia Telangiectasia [MESH:D001260] (142)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Language Disorders [MESH:D007806] (653)   Dyslexia [MESH:D004410] (17)  Learning Disorders [MESH:D007859] (2727)   Dyslexia [MESH:D004410] (15)  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)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Coffin-Siris syndrome [MESH:C536436] (102)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Adrenoleukodystrophy [MESH:D000326] (1348)  Psychomotor Disorders [MESH:D011596] (576)   Apraxias [MESH:D001072] (118)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypertonia [MESH:D009122] (775)  Spasm [MESH:D013035] (418)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  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)   Deafness [MESH:D003638] (623)  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)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Muscular Diseases [MESH:D009135] (3538)   Systemic carnitine deficiency [MESH:C536778] (92)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Distal Myopathies [MESH:D049310] (178)   Distal myopathy, Nonaka type [MESH:C536816] (40)  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)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Myositis, Inclusion Body [MESH:D018979] (103)   Inclusion body myopathy autosomal recessive [MESH:C538329] (40)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Corpus callosum agenesis neuronopathy [MESH:C536446] (20)  Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Mononeuropathies [MESH:D020422] (604)   Sciatic Neuropathy [MESH:D020426] (477)  Median Neuropathy [MESH:D020423] (153)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Nerve Compression Syndromes [MESH:D009408] (166)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4B2 [MESH:C535421] (10)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Neurotoxicity Syndromes [MESH:D020258] (4570)   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, Circadian Rhythm [MESH:D020178] (94)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82)  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)   Corneal Diseases [MESH:D003316] (1445)   Keratoconus [MESH:D007640] (121)  Corneal Opacity [MESH:D003318] (544)   Peters anomaly [MESH:C537884] (465)  Eye Abnormalities [MESH:D005124] (1233)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Peters anomaly [MESH:C537884] (465)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Retinitis Pigmentosa 13 [MESH:C564008] (30)  Eyelid Diseases [MESH:D005141] (882)   Blepharoptosis [MESH:D001763] (117)   Carnevale syndrome [MESH:C535586] (45)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma 3, Primary Congenital, A [MESH:C565547] (434)  Glaucoma, Open-Angle [MESH:D005902] (1281)   Glaucoma, Primary Open Angle [MESH:C562750] (466)  Glaucoma 1, Open Angle, A [MESH:C564234] (446)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Strabismus [MESH:D013285] (79)   Carnevale syndrome [MESH:C535586] (45)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinopathy of Prematurity [MESH:D012178] (353)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Retinitis Pigmentosa 13 [MESH:C564008] (30)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Uveal Diseases [MESH:D014603] (2428)   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)   Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)   Follicle-stimulating hormone deficiency, isolated [MESH:C537070] (185)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  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)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Urogenital Abnormalities [MESH:D014564] (2065)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency [MESH:C535978] (62)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  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)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Nephrosis [MESH:D009401] (2228)  Zellweger Syndrome [MESH:D015211] (182)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria [MESH:C563693] (17)  Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)   Medullary Cystic Kidney Disease 2 [MESH:C548033] (17)  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, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  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)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Renal hypouricemia [MESH:C537757] (71)  Hypouricemia, Renal, 2 [MESH:C567426] (32)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  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)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Polyuria [MESH:D011141] (279)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71) 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)   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)   Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Urogenital Abnormalities [MESH:D014564] (2043)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency [MESH:C535978] (62)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  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)  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)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Nephrosis [MESH:D009401] (2228)  Zellweger Syndrome [MESH:D015211] (182)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria [MESH:C563693] (17)  Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)   Medullary Cystic Kidney Disease 2 [MESH:C548033] (17)  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, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  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)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Renal hypouricemia [MESH:C537757] (71)  Hypouricemia, Renal, 2 [MESH:C567426] (32)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  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)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Polyuria [MESH:D011141] (279)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71)  Pregnancy Complications [MESH:D011248] (4768)   Diabetes, Gestational [MESH:D016640] (1157)  Fetal Death [MESH:D005313] (464)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Abortion, Spontaneous [MESH:D000022] (2780)   Abortion, Habitual [MESH:D000026] (32)  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)   Abruptio Placentae [MESH:D000037] (430)  Dystocia [MESH:D004420] (10)  Obstetric Labor, Premature [MESH:D007752] (1316)   Premature Birth [MESH:D047928] (118)  Placenta Diseases [MESH:D010922] (1781)   Abruptio Placentae [MESH:D000037] (430) 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)  Malpuech facial clefting syndrome [MESH:C535704] (45)  Ductus Arteriosus, Patent [MESH:D004374] (325)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 [MESH:C566471] (47)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  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)  Pericardial Effusion [MESH:D010490] (1015)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 2 [MESH:C567087] (15)  Cardiac Complexes, Premature [MESH:D005117] (429)   Ventricular Premature Complexes [MESH:D018879] (418)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1BB [MESH:C567877] (31)  Cardiomyopathies [MESH:D009202] (5331)   Systemic carnitine deficiency [MESH:C536778] (92)  Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  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, 10 [MESH:C565707] (31)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 [MESH:C566471] (47)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1BB [MESH:C567877] (31)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Malpuech facial clefting syndrome [MESH:C535704] (45)  Ductus Arteriosus, Patent [MESH:D004374] (325)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 [MESH:C566471] (47)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  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, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Vasospasm [MESH:D003329] (533)  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)   Arteritis [MESH:D001167] (1084)  Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Peripheral Vascular Diseases [MESH:D016491] (1412)  Retinal Vein Occlusion [MESH:D012170] (607)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Dissecting [MESH:D000784] (699)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Angioedema [MESH:D000799] (837)   Acquired angioedema [MESH:C538173] (157)  Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Mesenteric Vascular Occlusion [MESH:D008641] (147)  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)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Artery Thrombosis [MESH:D002341] (138)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   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)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Carotid Artery Thrombosis [MESH:D002341] (138)  Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  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)   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)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Thrombosis [MESH:D013927] (3101)   Heparin Cofactor II Deficiency [MESH:C562865] (45)  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)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Venous Thrombosis [MESH:D020246] (1141)   Budd-Chiari Syndrome [MESH:D006502] (164)  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 3 [MESH:C536196] (142)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Malignant [MESH:D006974] (621)  Hypertension, Pregnancy-Induced [MESH:D046110] (397)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  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, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Vasospasm [MESH:D003329] (533)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Telangiectasis [MESH:D013684] (255)   Ataxia Telangiectasia [MESH:D001260] (142)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084)  Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Z. Exceptions (453)   Not Fully Specified [NFS] (453)  Hematologic Diseases [MESH:D006402] (6174)   Methemoglobinemia [MESH:D008708] (850)  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 5 [MESH:C567280] (30)  Anemia, Hemolytic [MESH:D000743] (3083)   Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)  Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)  Anemia, Sickle Cell [MESH:D000755] (1722)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, Iron-Deficiency [MESH:D018798] (547)   Iron-Refractory Iron Deficiency Anemia [MESH:C562385] (20)  Anemia, Macrocytic [MESH:D000748] (382)   Anemia, Megaloblastic [MESH:D000749] (288)  Red-Cell Aplasia, Pure [MESH:D012010] (183)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 5 [MESH:C567280] (30)  Blood Coagulation Disorders [MESH:D001778] (1828)   Flaujeac factor deficiency [MESH:C537060] (117)  Disseminated Intravascular Coagulation [MESH:D004211] (462)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Factor V Deficiency [MESH:D005166] (61)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Coagulation Protein Disorders [MESH:D020147] (580)   Factor V Deficiency [MESH:D005166] (61)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Blood Protein Disorders [MESH:D001796] (3051)   Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   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 5 [MESH:C567280] (30)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Factor V Deficiency [MESH:D005166] (61)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Leukocyte Disorders [MESH:D007960] (2662)   Leukocytosis [MESH:D007964] (988)  Leukopenia [MESH:D007970] (1921)   Reticular dysgenesis [MESH:C538361] (49)  Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Thrombophilia [MESH:D019851] (592)   Thrombophilia, hereditary [MESH:C540694] (59)  Disseminated Intravascular Coagulation [MESH:D004211] (462)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Lymphatic Diseases [MESH:D008206] (5167)   Splenic Diseases [MESH:D013158] (1323)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) 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)   Abnormalities, Multiple [MESH:D000015] (3192)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Coffin-Siris syndrome [MESH:C536436] (102)  Basal Cell Nevus Syndrome [MESH:D001478] (67)  Bloom Syndrome [MESH:D001816] (107)  Costello Syndrome [MESH:D056685] (407)  Donohue Syndrome [MESH:D056731] (95)  Silver-Russell Syndrome [MESH:D056730] (142)  Zellweger Syndrome [MESH:D015211] (182)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 9 [MESH:C563659] (35)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Malpuech facial clefting syndrome [MESH:C535704] (45)  Ductus Arteriosus, Patent [MESH:D004374] (325)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 [MESH:C566471] (47)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  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)  Chromosome Disorders [MESH:D025063] (2030)   Silver-Russell Syndrome [MESH:D056730] (142)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 9 [MESH:C563659] (35)  Eye Abnormalities [MESH:D005124] (1233)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Peters anomaly [MESH:C537884] (465)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Microcephaly [MESH:D008831] (700)  Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 9 [MESH:C563659] (35)  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)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  Noonan Syndrome 5 [MESH:C548083] (169)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Hip Dislocation, Congenital [MESH:D006618] (56)   Carnevale syndrome [MESH:C535586] (45)  Limb Deformities, Congenital [MESH:D017880] (1813)   Foot Deformities, Congenital [MESH:D005532] (538)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Polydactyly [MESH:D017689] (318)   Holoprosencephaly 9 [MESH:C563659] (35)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Corpus callosum agenesis neuronopathy [MESH:C536446] (20)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 9 [MESH:C563659] (35)  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 4B2 [MESH:C535421] (10)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 9 [MESH:C563659] (35)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Skin Abnormalities [MESH:D012868] (1723)   Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Urogenital Abnormalities [MESH:D014564] (2064)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency [MESH:C535978] (62)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Angioedemas, Hereditary [MESH:D054179] (172)  Costello Syndrome [MESH:D056685] (407)  Donohue Syndrome [MESH:D056731] (95)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency [MESH:C535978] (62)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)  Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)  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 5 [MESH:C567280] (30)  Ataxia Telangiectasia [MESH:D001260] (142)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Factor V Deficiency [MESH:D005166] (61)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 2 [MESH:C567087] (15)  Chromosome Disorders [MESH:D025063] (2030)   Silver-Russell Syndrome [MESH:D056730] (142)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 9 [MESH:C563659] (35)  Dwarfism [MESH:D004392] (783)   Silver-Russell Syndrome [MESH:D056730] (142)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Retinitis Pigmentosa 13 [MESH:C564008] (30)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Adrenoleukodystrophy [MESH:D000326] (1348)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia musculorum deformans type 1 [MESH:C538005] (21)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4B2 [MESH:C535421] (10)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Adrenoleukodystrophy [MESH:D000326] (1348)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 28 [MESH:C537205] (13)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Dihydropyrimidinase Deficiency [MESH:C562815] (27)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Sarcosinemia [MESH:C537236] (38)  Methionine Adenosyltransferase Deficiency [MESH:C562681] (56)  Methylmalonic Aciduria and Homocystinuria, CblF Type [MESH:C564747] (21)  Hyperhomocysteinemia [MESH:D020138] (1724)  Phenylketonurias [MESH:D010661] (156)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Citrullinemia [MESH:D020159] (99)   Neonatal-onset citrullinemia type 2 [MESH:C536398] (35)  Adult-onset citrullinemia type 2 [MESH:C538053] (35)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Phenylketonurias [MESH:D010661] (156)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Peroxisomal Disorders [MESH:D018901] (1472)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease, Infantile [MESH:D052919] (51)  Zellweger Syndrome [MESH:D015211] (182)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Citrullinemia [MESH:D020159] (99)   Neonatal-onset citrullinemia type 2 [MESH:C536398] (35)  Adult-onset citrullinemia type 2 [MESH:C538053] (35)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Cytochrome-c Oxidase Deficiency [MESH:D030401] (48)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  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)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Peroxisomal Disorders [MESH:D018901] (1788)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease, Infantile [MESH:D052919] (51)  Zellweger Syndrome [MESH:D015211] (182)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Protoporphyria, Erythropoietic [MESH:D046351] (49)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Gout [MESH:D006073] (261)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Renal hypouricemia [MESH:C537757] (71)  Hypouricemia, Renal, 2 [MESH:C567426] (32)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency [MESH:C535978] (62)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Distal Myopathies [MESH:D049310] (178)   Distal myopathy, Nonaka type [MESH:C536816] (40)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Basal Cell Nevus Syndrome [MESH:D001478] (67)  Skin Diseases, Genetic [MESH:D012873] (3456)   dowling-degos disease [MESH:C562924] (53)  Dermatitis, Atopic [MESH:D003876] (2052)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Epidermolysis Bullosa [MESH:D004820] (259)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Protoporphyria, Erythropoietic [MESH:D046351] (49)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Ichthyosis [MESH:D007057] (476)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Retinopathy of Prematurity [MESH:D012178] (353)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Reticular dysgenesis [MESH:C538361] (49) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  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 3 [MESH:C536196] (142)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  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)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Skin Neoplasms [MESH:D012878] (2991)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Drug Eruptions [MESH:D003875] (2697)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Erythema [MESH:D004890] (1330)   Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Hair Diseases [MESH:D006201] (1891)   Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136)  Hypotrichosis [MESH:D007039] (1513)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Alopecia [MESH:D000505] (1453)  Keratosis [MESH:D007642] (1941)   Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   dowling-degos disease [MESH:C562924] (53)  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)  Skin Abnormalities [MESH:D012868] (1709)   Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  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)   dowling-degos disease [MESH:C562924] (53)  Dermatitis, Atopic [MESH:D003876] (2052)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Protoporphyria, Erythropoietic [MESH:D046351] (49)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Bacterial [MESH:D017192] (156)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Protoporphyria, Erythropoietic [MESH:D046351] (49)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   dowling-degos disease [MESH:C562924] (53)  Lichenoid Eruptions [MESH:D017512] (1324)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Acquired angioedema [MESH:C538173] (157)  Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Sweat Gland Diseases [MESH:D013543] (231)   Hidradenitis [MESH:D016575] (121)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Acid-Base Imbalance [MESH:D000137] (854)   Alkalosis [MESH:D000471] (384)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Phenylketonurias [MESH:D010661] (156)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Peroxisomal Disorders [MESH:D018901] (1472)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease, Infantile [MESH:D052919] (51)  Zellweger Syndrome [MESH:D015211] (182)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Citrullinemia [MESH:D020159] (99)   Neonatal-onset citrullinemia type 2 [MESH:C536398] (35)  Adult-onset citrullinemia type 2 [MESH:C538053] (35)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Hypercalcemia [MESH:D006934] (1999)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Bloom Syndrome [MESH:D001816] (107)  Fanconi Anemia [MESH:D005199] (1604)  Ataxia Telangiectasia [MESH:D001260] (142)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Reticular dysgenesis [MESH:C538361] (49)  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 Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Donohue Syndrome [MESH:D056731] (95)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  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)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Hypoglycemia [MESH:D007003] (2420)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Hyperinsulinemic Hypoglycemia, Familial, 5 [MESH:C566494] (94)  Iron Metabolism Disorders [MESH:D019189] (2139)   Anemia, Iron-Deficiency [MESH:D018798] (547)   Iron-Refractory Iron Deficiency Anemia [MESH:C562385] (20)  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 III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Hypertriglyceridemia [MESH:D015228] (808)   Hyperlipoproteinemia Type V [MESH:D006954] (37)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Xanthomatosis [MESH:D014973] (145)   Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)  Malabsorption Syndromes [MESH:D008286] (1869)   Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Dihydropyrimidinase Deficiency [MESH:C562815] (27)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Sarcosinemia [MESH:C537236] (38)  Methionine Adenosyltransferase Deficiency [MESH:C562681] (56)  Methylmalonic Aciduria and Homocystinuria, CblF Type [MESH:C564747] (21)  Hyperhomocysteinemia [MESH:D020138] (1724)  Phenylketonurias [MESH:D010661] (156)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Citrullinemia [MESH:D020159] (99)   Neonatal-onset citrullinemia type 2 [MESH:C536398] (35)  Adult-onset citrullinemia type 2 [MESH:C538053] (35)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Phenylketonurias [MESH:D010661] (156)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Peroxisomal Disorders [MESH:D018901] (1472)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease, Infantile [MESH:D052919] (51)  Zellweger Syndrome [MESH:D015211] (182)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Citrullinemia [MESH:D020159] (99)   Neonatal-onset citrullinemia type 2 [MESH:C536398] (35)  Adult-onset citrullinemia type 2 [MESH:C538053] (35)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  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)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Peroxisomal Disorders [MESH:D018901] (1788)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease, Infantile [MESH:D052919] (51)  Zellweger Syndrome [MESH:D015211] (182)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Protoporphyria, Erythropoietic [MESH:D046351] (49)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Gout [MESH:D006073] (261)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Renal hypouricemia [MESH:C537757] (71)  Hypouricemia, Renal, 2 [MESH:C567426] (32)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency [MESH:C535978] (62)  Mitochondrial Diseases [MESH:D028361] (2561)   Sarcosinemia [MESH:C537236] (38)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Cytochrome-c Oxidase Deficiency [MESH:D030401] (48)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  Leigh Disease [MESH:D007888] (206)   Leigh syndrome , French Canadian type [MESH:C537004] (35)  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)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Protoporphyria, Erythropoietic [MESH:D046351] (49)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Frontotemporal Lobar Degeneration [MESH:D057174] (308)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Protoporphyria, Erythropoietic [MESH:D046351] (49)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hypokalemia [MESH:D007008] (1041)  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 A Deficiency [MESH:D014802] (705)  Vitamin B Deficiency [MESH:D014804] (1817)   Folic Acid Deficiency [MESH:D005494] (134)  Hyperhomocysteinemia [MESH:D020138] (1716)  Vitamin B 12 Deficiency [MESH:D014806] (47)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Obesity, Abdominal [MESH:D056128] (115)  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)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency [MESH:C535978] (62)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Hypoaldosteronism [MESH:D006994] (104)   18-Hydroxylase deficiency [MESH:C537806] (98)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Hyperaldosteronism [MESH:D006929] (419)   Glucocorticoid-Remediable Aldosteronism [MESH:C563177] (62)  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)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  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)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Gonadal Disorders [MESH:D006058] (5088)   Hypogonadism [MESH:D007006] (1123)  Puberty, Delayed [MESH:D011628] (449)  Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency [MESH:C535978] (62)  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)   Carnevale syndrome [MESH:C535586] (45)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1259)   Hyperprolactinemia [MESH:D006966] (603)  Hypopituitarism [MESH:D007018] (732)   Holoprosencephaly 9 [MESH:C563659] (35)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Hyperthyroxinemia [MESH:D006981] (659)   Dystransthyretinemic Euthyroidal Hyperthyroxinemia [MESH:C567719] (136)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2695)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Anaphylaxis [MESH:D000707] (299)  Asthma, Aspirin-Induced [MESH:D055963] (1055)  Dermatitis, Atopic [MESH:D003876] (2052)  Food Hypersensitivity [MESH:D005512] (608)   Peanut Hypersensitivity [MESH:D021183] (572)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Asthma [MESH:D001249] (3914)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Acquired angioedema [MESH:C538173] (157)  Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   T cell immunodeficiency primary [MESH:C536780] (36)  Complement Component 4, Partial Deficiency Of [MESH:C565168] (55)  Lymphopenia [MESH:D008231] (990)  Ataxia Telangiectasia [MESH:D001260] (142)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Reticular dysgenesis [MESH:C538361] (49)  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)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  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) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Atrophy [MESH:D001284] (2603)  Plaque, Atherosclerotic [MESH:D058226] (696)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Corpus callosum agenesis neuronopathy [MESH:C536446] (20)  Calculi [MESH:D002137] (756)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Hypertrophy [MESH:D006984] (4476)   Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)   Colonic Polyps [MESH:D003111] (210)  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)  Ischemia [MESH:D007511] (3049)  Leukocytosis [MESH:D007964] (978)  Lithiasis [MESH:D020347] (345)  Necrosis [MESH:D009336] (4019)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Cardiac Complexes, Premature [MESH:D005117] (429)   Ventricular Premature Complexes [MESH:D018879] (418)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)  Embryo Loss [MESH:D020964] (288)  Fetal Death [MESH:D005313] (464)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Nicolaides Baraitser syndrome [MESH:C536116] (40)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Hyperammonemia [MESH:D022124] (322)   Systemic carnitine deficiency [MESH:C536778] (92)  Hyperuricemia [MESH:D033461] (82)   Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria [MESH:C563693] (17)  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)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Dysmenorrhea [MESH:D004412] (189)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)  Neoplastic Processes [MESH:D009385] (5317)   Anaplasia [MESH:D000708] (348)  Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  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)   Edema [MESH:D004487] (3726)  Feminization [MESH:D005262] (655)  Fetal Distress [MESH:D005316] (99)  Flushing [MESH:D005483] (506)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Birth Weight [MESH:D001724] (377)  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)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Apraxias [MESH:D001072] (114)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Communication Disorders [MESH:D003147] (2918)   Language Disorders [MESH:D007806] (653)   Dyslexia [MESH:D004410] (17)  Learning Disorders [MESH:D007859] (2727)   Dyslexia [MESH:D004410] (15)  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)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Coffin-Siris syndrome [MESH:C536436] (102)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Psychomotor Disorders [MESH:D011596] (576)   Apraxias [MESH:D001072] (118)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypertonia [MESH:D009122] (775)  Spasm [MESH:D013035] (418)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  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)   Deafness [MESH:D003638] (593)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Pelvic Pain [MESH:D017699] (198)   Dysmenorrhea [MESH:D004412] (189)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Nausea [MESH:D009325] (2300)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperoxia [MESH:D018496] (694)  Hyperventilation [MESH:D006985] (652)  Urological Manifestations [MESH:D020924] (3532)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Virilism [MESH:D014770] (327)   Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Sleep Disorders, Circadian Rhythm [MESH:D020178] (93)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82) 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)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2697)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Manganese Poisoning [MESH:D020149] (2214)  Neurotoxicity Syndromes [MESH:D020258] (3323)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Water Intoxication [MESH:D014869] (106)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Drug Overdose [MESH:D062787] (513)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholic Intoxication [MESH:D000435] (87)  Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950) 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)  Fractures, Bone [MESH:D050723] (597)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Sprains and Strains [MESH:D013180] (153)   Cumulative Trauma Disorders [MESH:D012090] (151)   Carpal Tunnel Syndrome [MESH:D002349] (147)  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, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Aromatic [MESH:D006841] (19108)   Benzene Derivatives [MESH:D001555] (10684)   Biphenyl Compounds [MESH:D001713] (678)   Polychlorinated Biphenyls [MESH:D011078] (104)  Hydrocarbons, Halogenated [MESH:D006846] (2296)   Hydrocarbons, Chlorinated [MESH:D006843] (491)   Polychlorinated Biphenyls [MESH:D011078] (112) 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)  Nicolaides Baraitser syndrome [MESH:C536116] (40) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Apraxias [MESH:D001072] (83)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Intellectual Disability [MESH:D008607] (1109)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Coffin-Siris syndrome [MESH:C536436] (102)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Psychomotor Disorders [MESH:D011596] (250)   Apraxias [MESH:D001072] (83)   Early-onset ataxia with oculomotor apraxia and hypoalbuminemia [MESH:C538013] (18)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Developmental Disabilities [MESH:D002658] (151)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Intellectual Disability [MESH:D008607] (1109)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Coffin-Siris syndrome [MESH:C536436] (102)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XX Disorders of Sex Development [MESH:D058489] (375)   Cortisone reductase deficiency [MESH:C536447] (136)  Sleep Disorders [MESH:D012893] (148)   Dyssomnias [MESH:D020920] (101)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (84)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82) G. Phenomena and Processes  G. Phenomena and Processes  Chemical Phenomena [MESH:D055598] (397)   Biochemical Phenomena [MESH:D001669] (328)   Molecular Structure [MESH:D015394] (174)   Base Sequence [MESH:D001483] (86)   Repetitive Sequences, Nucleic Acid [MESH:D012091] (58)   Tandem Repeat Sequences [MESH:D020080] (35)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Genetic Structures [MESH:D040342] (1612)   Base Sequence [MESH:D001483] (86)   Repetitive Sequences, Nucleic Acid [MESH:D012091] (57)   Tandem Repeat Sequences [MESH:D020080] (35)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Genome [MESH:D016678] (249)   Genome Components [MESH:D040481] (231)   DNA Sequence, Unstable [MESH:D043243] (28)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Tandem Repeat Sequences [MESH:D020080] (34)   DNA Repeat Expansion [MESH:D042622] (25)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  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)