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 Sulindac
D013467		 
  
  
  

MeSH Unique Identifier: D013467
Scope Notes: A sulfinylindene derivative prodrug whose sulfinyl moiety is converted in vivo to an active NSAID analgesic. Specifically, the prodrug is converted by liver enzymes to a sulfide which is excreted in the bile and then reabsorbed from the intestine. This helps to maintain constant blood levels with reduced gastrointestinal side effects.
Chemical – Gene Interaction

Note 1: Acetylcysteine inhibits the reaction [Sulindac results in increased expression of ABCC1 protein]

Note 2: Sulindac results in increased expression of ABCC1 protein

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C23. Pathological Conditions, Signs and Symptoms: Pathologic Processes [MESH:D010335] > Muscle Weakness [MESH:D018908] > Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006]
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1. Human Genes 
1. Human Genes
 Aldo-keto reductases [HGNC:AKR] (282) 
 aldo-keto reductase family 1, member C1 [HGNC:AKR1C1] (148)
 aldo-keto reductase family 1, member C2 [HGNC:AKR1C2] (134)
 aldo-keto reductase family 1, member C3 [HGNC:AKR1C3] (128)
 Ankyrin repeat domain containing [HGNC:ANKRD] (566) 
 ankyrin repeat domain 11 [HGNC:ANKRD11] (18)
 euchromatic histone-lysine N-methyltransferase 2 [HGNC:EHMT2] (14)
 integrin-linked kinase [HGNC:ILK] (17)
 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 [HGNC:NFKB1] (254)
 nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [HGNC:NFKBIA] (290)
 Armadillo repeat containing [HGNC:ARMC] (176) 
 catenin (cadherin-associated protein), beta 1, 88kDa [HGNC:CTNNB1] (129)
 ATPases [HGNC:ATP] (106) 
 ATPases, AAA [HGNC:AATP] (69) 
 origin recognition complex, subunit 4 [HGNC:ORC4] (8)
 ATP-binding cassette transporters [HGNC:ABC] (821) 
 ATP-binding cassette transporters, subfamily C [HGNC:ABCC] (458) 
 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 [HGNC:ABCC1] (177)
 ATP-binding cassette, sub-family C (CFTR/MRP), member 3 [HGNC:ABCC3] (89)
 Basic helix-loop-helix [HGNC:BHLH] (618) 
 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) [HGNC:HIF1A] (212)
 transcription factor 04 [HGNC:TCF4] (38)
 v-myc avian myelocytomatosis viral oncogene homolog [HGNC:MYC] (254)
 Basic leucine zipper proteins [HGNC:bZIP] (670) 
 jun D proto-oncogene [HGNC:JUND] (61)
 X-box binding protein 1 [HGNC:XBP1] (79)
 Beta 3-glycosyltransferases [HGNC:B3GT] (48) 
 LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [HGNC:LFNG] (14)
 Cadherins [HGNC:CDH] (214) 
 Cadherins, related [HGNC:CDHR] (55) 
 ret proto-oncogene [HGNC:RET] (37)
 Cathepsins [HGNC:CTS] (135) 
 cathepsin B [HGNC:CTSB] (48)
 CD molecules [HGNC:CD] (1459) 
 hyaluronan-mediated motility receptor (RHAMM) [HGNC:HMMR] (41)
 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) [HGNC:ITGA2] (42)
 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) [HGNC:ITGB3] (49)
 integrin, beta 4 [HGNC:ITGB4] (41)
 intercellular adhesion molecule 1 [HGNC:ICAM1] (286)
 tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155)
 tumor necrosis factor receptor superfamily, member 10b [HGNC:TNFRSF10B] (124)
 Chemokine ligands [HGNC:CCL] (472) 
 chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141)
 Cyclin-dependent kinases [HGNC:CDK] (338) 
 cyclin-dependent kinase 01 [HGNC:CDK1] (151)
 cyclin-dependent kinase 02 [HGNC:CDK2] (177)
 cyclin-dependent kinase 04 [HGNC:CDK4] (127)
 cyclin-dependent kinase 06 [HGNC:CDK6] (55)
 Cytochrome P450s [HGNC:CYP] (1673) 
 cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566)
 cytochrome P450, family 01, subfamily A, polypeptide 02 [HGNC:CYP1A2] (466)
 cytochrome P450, family 01, subfamily B, polypeptide 01 [HGNC:CYP1B1] (301)
 Endogenous Ligands [HGNC:ENDOLIG] (1191) 
 chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141)
 galanin/GMAP prepropeptide [HGNC:GAL] (26)
 Fibronectin type III domain containing [HGNC:FN3] (399) 
 integrin, beta 4 [HGNC:ITGB4] (41)
 Histones [HGNC:HIST] (173) 
 Histones, Replication-independent [HGNC:RIH] (148) 
 H2A histone family, member X [HGNC:H2AFX] (129)
 Immunoglobulin superfamily domain containing [HGNC:IGSF] (761) 
 Immunoglobulin-like domain containing [HGNC:IGD] (645) 
 intercellular adhesion molecule 1 [HGNC:ICAM1] (286)
 Integrins [HGNC:ITG] (284) 
 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) [HGNC:ITGA2] (42)
 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) [HGNC:ITGB3] (49)
 integrin, beta 4 [HGNC:ITGB4] (41)
 Interleukins and interleukin receptors [HGNC:IL] (1294) 
 interleukin 01, beta [HGNC:IL1B] (497)
 interleukin 24 [HGNC:IL24] (37)
 interleukin 32 [HGNC:IL32] (26)
 K-methyltransferases [HGNC:KMT] (101) 
 euchromatic histone-lysine N-methyltransferase 2 [HGNC:EHMT2] (14)
 Lectins, galactoside-binding [HGNC:LGALS] (92) 
 lectin, galactoside-binding, soluble, 3 [HGNC:LGALS3] (39)
 Mitogen-activated protein kinase cascade [HGNC:MAP#K] (854) 
 Mitogen-activated protein kinases [HGNC:MAPK] (797) 
 mitogen-activated protein kinase 01 [HGNC:MAPK1] (651)
 mitogen-activated protein kinase 03 [HGNC:MAPK3] (644)
 mitogen-activated protein kinase 08 [HGNC:MAPK8] (234)
 Nuclear hormone receptors [HGNC:NR] (1322) 
 peroxisome proliferator-activated receptor delta [HGNC:PPARD] (67)
 Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227) 
 pleckstrin homology domain containing, family F (with FYVE domain) member 1 [HGNC:PLEKHF1] (15)
 Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225) 
 Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155) 
 aurora kinase A [HGNC:AURKA] (52)
 Proteoglycans [HGNC:proteoglycan] (70) 
 Proteoglycans, extracellular matrix: small leucine-rich repeats [HGNC:SLRR] (37) 
 decorin [HGNC:DCN] (27)
 RING-type zinc fingers [HGNC:RNF] (151) 
 promyelocytic leukemia [HGNC:PML] (30)
 tripartite motif containing 02 [HGNC:TRIM2] (22)
 SH2 domain containing [HGNC:SH2D] (431) 
 c-src tyrosine kinase [HGNC:CSK] (15)
 SHC (Src homology 2 domain containing) transforming protein 1 [HGNC:SHC1] (29)
 signal transducer and activator of transcription 3 (acute-phase response factor) [HGNC:STAT3] (145)
 v-src avian sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog [HGNC:SRC] (88)
 Solute carriers [HGNC:SLC] (716) 
 solute carrier family 07 (cationic amino acid transporter, y+ system), member 01 [HGNC:SLC7A1] (23)
 solute carrier family 22 (organic cation transporter), member 01 [HGNC:SLC22A1] (52)
 solute carrier family 22 (organic cation transporter), member 02 [HGNC:SLC22A2] (31)
 solute carrier family 22 (organic anion transporter), member 06 [HGNC:SLC22A6] (72)
 solute carrier family 30 (zinc transporter), member 1 [HGNC:SLC30A1] (46)
 Sulfotransferases, cytosolic [HGNC:SULT] (167) 
 sulfotransferase family 1E, estrogen-preferring, member 1 [HGNC:SULT1E1] (49)
 T-boxes [HGNC:TBX] (49) 
 T-box 03 [HGNC:TBX3] (24)
 Transglutaminases [HGNC:TGM] (82) 
 transglutaminase 2 [HGNC:TGM2] (60)
 Transient receptor potential cation channels [HGNC:TRP] (169) 
 polycystic kidney disease 1 (autosomal dominant) [HGNC:PKD1] (10)
 Tripartite motif containing [HGNC:TRIM] (80) 
 promyelocytic leukemia [HGNC:PML] (30)
 tripartite motif containing 02 [HGNC:TRIM2] (22)
 Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898) 
 tumor necrosis factor [HGNC:TNF] (795)
 tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155)
 Tumor necrosis factor receptor superfamily [HGNC:TNFRSF] (295) 
 tumor necrosis factor receptor superfamily, member 10b [HGNC:TNFRSF10B] (124)
 UDP glucuronosyltransferases [HGNC:UGT] (298) 
 UDP glucuronosyltransferase 1 family, polypeptide A1 [HGNC:UGT1A1] (167)
 UDP glucuronosyltransferase 1 family, polypeptide A3 [HGNC:UGT1A3] (94)
 UDP glucuronosyltransferase 2 family, polypeptide B07 [HGNC:UGT2B7] (85)
 ZINC FINGERS [HGNC:ZNF] (383) 
 Other zinc fingers [HGNC:] (148) 
 Zinc fingers, FYVE-type [HGNC:ZFYVE ] (31) 
 pleckstrin homology domain containing, family F (with FYVE domain) member 1 [HGNC:PLEKHF1] (15)
2. Interaction: Human Genes and Chemicals 
2. Interaction: Human Genes and Chemicals
 Affects (3990) 
 binding (2423)
 cotreatment (1499)
 expression (494)
 localization (731)
 metabolic processing (485)
 reaction (624)
 response to substance (623)
 Decreases (5154) 
 activity (2549)
 degradation (120)
 expression (2187)
 metabolic processing (88)
 phosphorylation (590)
 reaction (3393)
 Increases (5571) 
 abundance (630)
 activity (2865)
 chemical synthesis (464)
 cleavage (666)
 degradation (347)
 expression (3238)
 glucuronidation (189)
 localization (244)
 metabolic processing (740)
 phosphorylation (1060)
 reaction (1574)
 response to substance (641)
A. Anatomy 
A. Anatomy
 Body Regions [MESH:D001829] (867) 
 Head [MESH:D006257] (523) 
 Ear [MESH:D004423] (236) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Musculoskeletal System [MESH:D009141] (1255) 
 Skeleton [MESH:D012863] (1177) 
 Bone and Bones [MESH:D001842] (1112) 
 Bones of Lower Extremity [MESH:D050281] (278) 
 Leg Bones [MESH:D007867] (228) 
 Patella [MESH:D010329] (168) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Bones of Upper Extremity [MESH:D001133] (240) 
 Arm Bones [MESH:D050280] (183) 
 Ulna [MESH:D014457] (96) 
 Ulnar-mammary syndrome [MESH:C536937] (57)
 Urogenital System [MESH:D014566] (986) 
 Urinary Tract [MESH:D014551] (721) 
 Kidney [MESH:D007668] (707) 
 Hereditary renal agenesis [MESH:C536482] (89)
 Nephrons [MESH:D009399] (518) 
 Kidney Tubules [MESH:D007684] (510) 
 Kidney Tubules, Proximal [MESH:D007687] (504) 
 Allanson Pantzar McLeod syndrome [MESH:C537048] (503)
 Cardiovascular System [MESH:D002319] (1086) 
 Heart [MESH:D006321] (904) 
 Heart Valves [MESH:D006351] (666) 
 Aortic Valve [MESH:D001021] (659) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Sense Organs [MESH:D012679] (1060) 
 Ear [MESH:D004423] (323) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Eye [MESH:D005123] (858) 
 Anterior Eye Segment [MESH:D000869] (664) 
 Peters anomaly [MESH:C537884] (465)
 Retina [MESH:D012160] (85) 
 Joubert syndrome 1 [MESH:C536293] (20)
 Cells [MESH:D002477] (1885) 
 Cellular Structures [MESH:D022082] (1562) 
 Chromosomes [MESH:D002875] (1300) 
 Chromosomes, Mammalian [MESH:D033481] (1282) 
 Chromosomes, Human [MESH:D002877] (1280) 
 Chromosomes, Human, 16-18 [MESH:D002902] (799) 
 Chromosomes, Human, Pair 17 [MESH:D002886] (779) 
 Chromosome 17 deletion [MESH:C538045] (769)
C01. Bacterial Infections and Mycoses 
C01. Bacterial Infections and Mycoses
 Bacterial Infections [MESH:D001424] (3716) 
 Bacteremia [MESH:D016470] (208)
 Gram-Negative Bacterial Infections [MESH:D016905] (3085) 
 Helicobacter Infections [MESH:D016481] (579)
 Chlamydiaceae Infections [MESH:D002694] (1699) 
 Chlamydia Infections [MESH:D002690] (1696)
 Enterobacteriaceae Infections [MESH:D004756] (669) 
 Salmonella Infections [MESH:D012480] (620) 
 Salmonella Infections, Animal [MESH:D012481] (604)
 Legionellosis [MESH:D007876] (612) 
 Legionnaires' Disease [MESH:D007877] (611)
 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) 
 Leprosy [MESH:D007918] (261)
 Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711) 
 Chlamydia Infections [MESH:D002690] (1693)
 Infection [MESH:D007239] (4109) 
 Arthritis, Infectious [MESH:D001170] (1702)
 Intraabdominal Infections [MESH:D059413] (958) 
 Appendicitis [MESH:D001064] (774)
 Peritonitis [MESH:D010538] (800)
 Opportunistic Infections [MESH:D009894] (949) 
 AIDS-Related Opportunistic Infections [MESH:D017088] (944) 
 AIDS-related Kaposi sarcoma [MESH:C554498] (914)
 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)
 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) 
 Papillomavirus Infections [MESH:D030361] (630)
 Hepadnaviridae Infections [MESH:D018347] (977) 
 Hepatitis B [MESH:D006509] (976)
 Herpesviridae Infections [MESH:D006566] (1944) 
 Epstein-Barr Virus Infections [MESH:D020031] (695) 
 Burkitt Lymphoma [MESH:D002051] (691)
 Sarcoma, Kaposi [MESH:D012514] (1578) 
 AIDS-related Kaposi sarcoma [MESH:C554498] (914)
 Hepatitis, Viral, Human [MESH:D006525] (1766) 
 Hepatitis B [MESH:D006509] (976)
 Hepatitis C [MESH:D006526] (1627)
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Opportunistic Infections [MESH:D009894] (949) 
 AIDS-Related Opportunistic Infections [MESH:D017088] (944) 
 AIDS-related Kaposi sarcoma [MESH:C554498] (914)
 RNA Virus Infections [MESH:D012327] (4215) 
 Flaviviridae Infections [MESH:D018178] (1656) 
 Hepatitis C [MESH:D006526] (1627)
 Mononegavirales Infections [MESH:D018701] (900) 
 Paramyxoviridae Infections [MESH:D018184] (889) 
 Pneumovirus Infections [MESH:D018186] (853) 
 Respiratory Syncytial Virus Infections [MESH:D018357] (852)
 Orthomyxoviridae Infections [MESH:D009976] (1077) 
 Influenza, Human [MESH:D007251] (1075)
 Picornaviridae Infections [MESH:D010850] (1672) 
 Cardiovirus Infections [MESH:D018188] (1548)
 Retroviridae Infections [MESH:D012192] (3420) 
 Lentivirus Infections [MESH:D016180] (3408) 
 HIV Infections [MESH:D015658] (3402) 
 Acquired Immunodeficiency Syndrome [MESH:D000163] (743)
 HIV Seropositivity [MESH:D006679] (480)
 HIV Wasting Syndrome [MESH:D019247] (1956)
 AIDS-Related Opportunistic Infections [MESH:D017088] (944) 
 AIDS-related Kaposi sarcoma [MESH:C554498] (914)
 Sexually Transmitted Diseases [MESH:D012749] (3305) 
 Sexually Transmitted Diseases, Viral [MESH:D015229] (3304) 
 HIV Infections [MESH:D015658] (3296) 
 Acquired Immunodeficiency Syndrome [MESH:D000163] (743)
 HIV Seropositivity [MESH:D006679] (480)
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Slow Virus Diseases [MESH:D012897] (782) 
 Acquired Immunodeficiency Syndrome [MESH:D000163] (743)
 Tumor Virus Infections [MESH:D014412] (1069) 
 Papillomavirus Infections [MESH:D030361] (537)
 Epstein-Barr Virus Infections [MESH:D020031] (693) 
 Burkitt Lymphoma [MESH:D002051] (691)
C03. Parasitic Diseases 
C03. Parasitic Diseases
 Parasitic Diseases [MESH:D010272] (3828) 
 Liver Diseases, Parasitic [MESH:D008109] (1009)
 Helminthiasis [MESH:D006373] (1644) 
 Nematode Infections [MESH:D009349] (870) 
 Adenophorea Infections [MESH:D017188] (808) 
 Enoplida Infections [MESH:D017189] (807) 
 Trichuriasis [MESH:D014257] (805)
 Trematode Infections [MESH:D014201] (1182) 
 Schistosomiasis [MESH:D012552] (1073) 
 Schistosomiasis mansoni [MESH:D012555] (1033)
 Opportunistic Infections [MESH:D009894] (949) 
 AIDS-Related Opportunistic Infections [MESH:D017088] (944) 
 AIDS-related Kaposi sarcoma [MESH:C554498] (914)
 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, Visceral [MESH:D007898] (2149)
 Leishmaniasis, Cutaneous [MESH:D016773] (2359) 
 Leishmaniasis, Mucocutaneous [MESH:D007897] (606)
 Skin Diseases, Parasitic [MESH:D012876] (2541) 
 Leishmaniasis [MESH:D007896] (2516) 
 Leishmaniasis, Cutaneous [MESH:D016773] (2359) 
 Leishmaniasis, Mucocutaneous [MESH:D007897] (606)
C04. Neoplasms 
C04. Neoplasms
 Neoplasms [MESH:D009369] (10293) 
 Neoplasms, Second Primary [MESH:D016609] (518)
 Cysts [MESH:D003560] (2625) 
 Ovarian Cysts [MESH:D010048] (2534) 
 Polycystic Ovary Syndrome [MESH:D011085] (2186)
 Hamartoma [MESH:D006222] (1484) 
 Tuberous Sclerosis [MESH:D014402] (635)
 Neoplasms by Histologic Type [MESH:D009370] (8793) 
 Leukemia [MESH:D007938] (4576) 
 Leukemia, Lymphoid [MESH:D007945] (3047) 
 Leukemia, T-Cell [MESH:D015458] (395)
 Leukemia, B-Cell [MESH:D015448] (2564) 
 Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
 Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) 
 Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)
 Leukemia, Myeloid [MESH:D007951] (2773) 
 Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)
 Leukemia, Myeloid, Acute [MESH:D015470] (2176) 
 Leukemia, Megakaryoblastic, Acute [MESH:D007947] (279)
 Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)
 Lymphoma [MESH:D008223] (3686) 
 Hodgkin Disease [MESH:D006689] (1082)
 Lymphoma, Non-Hodgkin [MESH:D008228] (3337) 
 Burkitt Lymphoma [MESH:D002051] (691)
 Lymphoma, Follicular [MESH:D008224] (1025)
 Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)
 Lymphoma, Mantle-Cell [MESH:D020522] (561)
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Burkitt Lymphoma [MESH:D002051] (691)
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Lymphoma, T-Cell [MESH:D016399] (1405) 
 Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)
 Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)
 Neoplasms, Complex and Mixed [MESH:D018193] (1121) 
 Carcinosarcoma [MESH:D002296] (581)
 Hepatoblastoma [MESH:D018197] (548)
 Wilms Tumor [MESH:D009396] (553)
 Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742) 
 Neoplasms, Adipose Tissue [MESH:D018205] (677) 
 Liposarcoma [MESH:D008080] (612) 
 Liposarcoma, Myxoid [MESH:D018208] (358)
 Neoplasms, Connective Tissue [MESH:D009372] (3626) 
 Sarcoma, Synovial [MESH:D013584] (993)
 Chondrosarcoma [MESH:D002813] (1217) 
 Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)
 Mastocytosis [MESH:D008415] (792) 
 Mastocytosis, Systemic [MESH:D034721] (769)
 Neoplasms, Bone Tissue [MESH:D018213] (2217) 
 Osteosarcoma [MESH:D012516] (2175)
 Neoplasms, Fibrous Tissue [MESH:D018218] (1720) 
 Fibroma [MESH:D005350] (1578) 
 Fibromatosis, Abdominal [MESH:D018221] (56)
 Fibromatosis, Aggressive [MESH:D018222] (1562) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Neoplasms, Muscle Tissue [MESH:D009379] (1965) 
 Leiomyosarcoma [MESH:D007890] (977)
 Smooth Muscle Tumor [MESH:D018235] (132)
 Sarcoma [MESH:D012509] (4246) 
 Carcinosarcoma [MESH:D002296] (581)
 Hemangiosarcoma [MESH:D006394] (1836)
 Leiomyosarcoma [MESH:D007890] (977)
 Osteosarcoma [MESH:D012516] (2175)
 Sarcoma, Synovial [MESH:D013584] (993)
 Chondrosarcoma [MESH:D002813] (1217) 
 Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)
 Liposarcoma [MESH:D008080] (612) 
 Liposarcoma, Myxoid [MESH:D018208] (358)
 Sarcoma, Kaposi [MESH:D012514] (1578) 
 AIDS-related Kaposi sarcoma [MESH:C554498] (914)
 Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126) 
 Neuroectodermal Tumors [MESH:D017599] (5066) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Retinoblastoma [MESH:D012175] (319)
 Glioma [MESH:D005910] (4261) 
 Medulloblastoma [MESH:D008527] (1282)
 Astrocytoma [MESH:D001254] (2692) 
 Melanoma astrocytoma syndrome [MESH:C536149] (159)
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Medulloblastoma [MESH:D008527] (1282)
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neuroendocrine Tumors [MESH:D018358] (3633) 
 Carcinoma, Neuroendocrine [MESH:D018278] (262) 
 Carcinoma, Medullary [MESH:D018276] (181) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Melanoma [MESH:D008545] (3508) 
 Melanoma astrocytoma syndrome [MESH:C536149] (159)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Paraganglioma [MESH:D010235] (297) 
 Pheochromocytoma [MESH:D010673] (275)
 Neoplasms, Glandular and Epithelial [MESH:D009375] (7760) 
 Adenoma [MESH:D000236] (4051) 
 Adenoma, Liver Cell [MESH:D018248] (685)
 Mesothelioma [MESH:D008654] (2567)
 Adenomatous Polyps [MESH:D018256] (1571) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Carcinoma [MESH:D002277] (7263) 
 Pancreatic cancer, adult [MESH:C535836] (572)
 Carcinoma, Basal Cell [MESH:D002280] (1628)
 Carcinoma, Small Cell [MESH:D018288] (1317)
 Carcinoma, Transitional Cell [MESH:D002295] (2662)
 Adenocarcinoma [MESH:D000230] (6565) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Adenocarcinoma, Clear Cell [MESH:D018262] (1291)
 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)
 Adrenocortical Carcinoma [MESH:D018268] (821) 
 Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)
 Carcinoma, Ductal [MESH:D044584] (1786) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Carcinoma, Neuroendocrine [MESH:D018278] (262) 
 Carcinoma, Medullary [MESH:D018276] (181) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 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)
 Bowen's Disease [MESH:D001913] (247)
 Neoplasms, Basal Cell [MESH:D018295] (1707) 
 Carcinoma, Basal Cell [MESH:D002280] (1628)
 Pilomatrixoma [MESH:D018296] (252)
 Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831) 
 Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)
 Carcinoma, Ductal [MESH:D044584] (1786) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Carcinoma, Medullary [MESH:D018276] (181) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Neoplasms, Mesothelial [MESH:D018301] (2569) 
 Mesothelioma [MESH:D008654] (2567)
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Retinoblastoma [MESH:D012175] (319)
 Glioma [MESH:D005910] (4261) 
 Medulloblastoma [MESH:D008527] (1282)
 Astrocytoma [MESH:D001254] (2692) 
 Melanoma astrocytoma syndrome [MESH:C536149] (159)
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Medulloblastoma [MESH:D008527] (1282)
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neoplasms, Squamous Cell [MESH:D018307] (4457) 
 Papilloma [MESH:D010212] (2243)
 Carcinoma, Squamous Cell [MESH:D002294] (4294) 
 Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Bowen's Disease [MESH:D001913] (247)
 Neoplasms, Nerve Tissue [MESH:D009380] (5201) 
 Meningioma [MESH:D008579] (978)
 Nerve Sheath Neoplasms [MESH:D018317] (365)
 Neuroectodermal Tumors [MESH:D017599] (5059) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Retinoblastoma [MESH:D012175] (319)
 Glioma [MESH:D005910] (4261) 
 Medulloblastoma [MESH:D008527] (1282)
 Astrocytoma [MESH:D001254] (2692) 
 Melanoma astrocytoma syndrome [MESH:C536149] (159)
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Medulloblastoma [MESH:D008527] (1282)
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neuroendocrine Tumors [MESH:D018358] (3625) 
 Carcinoma, Neuroendocrine [MESH:D018278] (184) 
 Carcinoma, Medullary [MESH:D018276] (181) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Melanoma [MESH:D008545] (3508) 
 Melanoma astrocytoma syndrome [MESH:C536149] (159)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Paraganglioma [MESH:D010235] (297) 
 Pheochromocytoma [MESH:D010673] (275)
 Neoplasms, Plasma Cell [MESH:D054219] (2772) 
 Multiple Myeloma [MESH:D009101] (2767)
 Neoplasms, Vascular Tissue [MESH:D009383] (2959) 
 Hemangiosarcoma [MESH:D006394] (1836)
 Meningioma [MESH:D008579] (978)
 Hemangioma [MESH:D006391] (690) 
 Hemangioma, Capillary [MESH:D018324] (503) 
 Hemangioblastoma [MESH:D018325] (395)
 Sarcoma, Kaposi [MESH:D012514] (1578) 
 AIDS-related Kaposi sarcoma [MESH:C554498] (914)
 Nevi and Melanomas [MESH:D018326] (3572) 
 Melanoma [MESH:D008545] (3508) 
 Melanoma astrocytoma syndrome [MESH:C536149] (159)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Nevus [MESH:D009506] (340) 
 Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)
 Neoplasms by Site [MESH:D009371] (9169) 
 Bone Neoplasms [MESH:D001859] (1334)
 Soft Tissue Neoplasms [MESH:D012983] (2003)
 Abdominal Neoplasms [MESH:D000008] (74) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Breast Neoplasms [MESH:D001943] (6077) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 Digestive System Neoplasms [MESH:D004067] (7487) 
 Biliary Tract Neoplasms [MESH:D001661] (1165) 
 Gallbladder Neoplasms [MESH:D005706] (993)
 Gastrointestinal Neoplasms [MESH:D005770] (6452) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Intestinal Neoplasms [MESH:D007414] (5358) 
 Cecal Neoplasms [MESH:D002430] (822)
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Turcot syndrome [MESH:C536928] (159)
 Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)
 Rectal Neoplasms [MESH:D012004] (717)
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Liver Neoplasms [MESH:D008113] (6048) 
 Adenoma, Liver Cell [MESH:D018248] (685)
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Pancreatic cancer, adult [MESH:C535836] (572)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Pituitary Neoplasms [MESH:D010911] (981)
 Adrenal Gland Neoplasms [MESH:D000310] (917) 
 Adrenal Cortex Neoplasms [MESH:D000306] (823) 
 Adrenocortical Carcinoma [MESH:D018268] (821) 
 Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)
 Multiple Endocrine Neoplasia [MESH:D009377] (375) 
 Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)
 Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)
 Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Ovarian Neoplasms [MESH:D010051] (3275) 
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Pancreatic cancer, adult [MESH:C535836] (572)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Thyroid Neoplasms [MESH:D013964] (2040) 
 Thyroid cancer, anaplastic [MESH:C536910] (489)
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Thyroid cancer, medullary [MESH:C536914] (74)
 Eye Neoplasms [MESH:D005134] (400) 
 Retinal Neoplasms [MESH:D019572] (320) 
 Retinoblastoma [MESH:D012175] (319)
 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)
 Otorhinolaryngologic Neoplasms [MESH:D010039] (1557) 
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500) 
 Nasopharyngeal carcinoma [MESH:C538339] (1198)
 Thyroid Neoplasms [MESH:D013964] (2040) 
 Thyroid cancer, anaplastic [MESH:C536910] (489)
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Thyroid cancer, medullary [MESH:C536914] (74)
 Mammary Neoplasms, Animal [MESH:D015674] (3404) 
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 Nervous System Neoplasms [MESH:D009423] (3130) 
 Melanoma astrocytoma syndrome [MESH:C536149] (159)
 Central Nervous System Neoplasms [MESH:D016543] (3055) 
 Brain Neoplasms [MESH:D001932] (2764) 
 Turcot syndrome [MESH:C536928] (159)
 Cerebral Ventricle Neoplasms [MESH:D002551] (772) 
 Choroid Plexus Neoplasms [MESH:D016545] (771) 
 Papilloma, Choroid Plexus [MESH:D020288] (769)
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Meningeal Neoplasms [MESH:D008577] (984) 
 Meningioma [MESH:D008579] (978)
 Skin Neoplasms [MESH:D012878] (2992) 
 Sebaceous Gland Neoplasms [MESH:D012626] (154)
 Thoracic Neoplasms [MESH:D013899] (6032) 
 Thymus Neoplasms [MESH:D013953] (247)
 Respiratory Tract Neoplasms [MESH:D012142] (6020) 
 Lung Neoplasms [MESH:D008175] (6015) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Bronchial Neoplasms [MESH:D001984] (3608) 
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Small Cell Lung Carcinoma [MESH:D055752] (1380)
 Urogenital Neoplasms [MESH:D014565] (7002) 
 Genital Neoplasms, Female [MESH:D005833] (2540) 
 Uterine Neoplasms [MESH:D014594] (2431) 
 Endometrial Neoplasms [MESH:D016889] (1987)
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Neoplasms [MESH:D011471] (6135)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Ureteral Neoplasms [MESH:D014516] (574)
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Wilms Tumor [MESH:D009396] (553)
 Neoplasms, Experimental [MESH:D009374] (5218) 
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 Tumor Virus Infections [MESH:D014412] (697) 
 Epstein-Barr Virus Infections [MESH:D020031] (693) 
 Burkitt Lymphoma [MESH:D002051] (691)
 Neoplasms, Multiple Primary [MESH:D009378] (961) 
 Tuberous Sclerosis [MESH:D014402] (635)
 Multiple Endocrine Neoplasia [MESH:D009377] (375) 
 Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)
 Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)
 Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 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) 
 Turcot syndrome [MESH:C536928] (159)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 Li-Fraumeni Syndrome [MESH:D016864] (859)
 Tuberous Sclerosis [MESH:D014402] (635)
 Wilms Tumor [MESH:D009396] (553)
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Multiple Endocrine Neoplasia [MESH:D009377] (375) 
 Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)
 Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)
 Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Precancerous Conditions [MESH:D011230] (2858) 
 Aberrant Crypt Foci [MESH:D058739] (326)
 Leukoplakia [MESH:D007971] (922) 
 Leukoplakia, Oral [MESH:D007972] (921)
 Xeroderma Pigmentosum [MESH:D014983] (213) 
 Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)
 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)
 Osteitis Deformans [MESH:D010001] (287)
 Bone Diseases, Developmental [MESH:D001848] (3315) 
 Acromicric dysplasia [MESH:C535662] (520)
 Dwarfism [MESH:D004392] (778) 
 Laron Syndrome [MESH:D046150] (91)
 Cockayne Syndrome [MESH:D003057] (107) 
 Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)
 Dwarfism, Pituitary [MESH:D004393] (235) 
 Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)
 Osteochondrodysplasias [MESH:D010009] (2440) 
 Camurati-Engelmann Syndrome [MESH:D003966] (492)
 Fibrous Dysplasia of Bone [MESH:D005357] (737)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 Bone Diseases, Endocrine [MESH:D001849] (747) 
 Dwarfism, Pituitary [MESH:D004393] (235) 
 Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)
 Bone Diseases, Metabolic [MESH:D001851] (3492) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Osteoporosis [MESH:D010024] (3037) 
 Osteoporosis, Postmenopausal [MESH:D015663] (2351)
 Bone Resorption [MESH:D001862] (2352) 
 Osteolysis [MESH:D010014] (1787)
 Spinal Diseases [MESH:D013122] (2485) 
 Intervertebral Disc Degeneration [MESH:D055959] (827)
 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)
 Jaw Diseases [MESH:D007571] (1601) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Joint Diseases [MESH:D007592] (4657) 
 Arthralgia [MESH:D018771] (191)
 Arthritis [MESH:D001168] (4416) 
 Arthritis, Experimental [MESH:D001169] (3142)
 Arthritis, Infectious [MESH:D001170] (1702)
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Osteoarthritis [MESH:D010003] (1743)
 Spondylarthritis [MESH:D025241] (1912) 
 Spondylarthropathies [MESH:D025242] (1909) 
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Contracture [MESH:D003286] (296) 
 Bethlem myopathy [MESH:C535436] (108)
 Muscular Diseases [MESH:D009135] (4071) 
 Muscle Cramp [MESH:D009120] (135)
 Contracture [MESH:D003286] (303) 
 Bethlem myopathy [MESH:C535436] (108)
 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)
 Muscle Weakness [MESH:D018908] (478) 
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 Muscular Disorders, Atrophic [MESH:D020966] (1598) 
 Muscular Dystrophies [MESH:D009136] (1593) 
 Bethlem myopathy [MESH:C535436] (108)
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Muscular Dystrophy, Duchenne [MESH:D020388] (942)
 Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
 Myopathies, Structural, Congenital [MESH:D020914] (272) 
 Myosclerosis, Autosomal Recessive [MESH:C564968] (45)
 Myositis [MESH:D009220] (2071) 
 Dermatomyositis [MESH:D003882] (1826)
 Polymyositis [MESH:D017285] (2007) 
 Dermatomyositis [MESH:D003882] (1826)
 Myotonic Disorders [MESH:D020967] (138) 
 Myotonia Congenita [MESH:D009224] (79) 
 Brody myopathy [MESH:C536607] (40)
 Musculoskeletal Abnormalities [MESH:D009139] (3796) 
 Craniofacial Abnormalities [MESH:D019465] (3098) 
 Costello Syndrome [MESH:D056685] (407)
 Microcephaly [MESH:D008831] (700)
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Limb Deformities, Congenital [MESH:D017880] (1813) 
 Acromicric dysplasia [MESH:C535662] (520)
 Rheumatic Diseases [MESH:D012216] (4032) 
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Osteoarthritis [MESH:D010003] (1743)
C06. Digestive System Diseases 
C06. Digestive System Diseases
 Digestive System Diseases [MESH:D004066] (9461) 
 Biliary Tract Diseases [MESH:D001660] (3845) 
 Cholelithiasis [MESH:D002769] (373)
 Bile Duct Diseases [MESH:D001649] (3512) 
 Cholangitis [MESH:D002761] (203)
 Cholestasis [MESH:D002779] (3419) 
 Cholestasis, Intrahepatic [MESH:D002780] (1510) 
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 Biliary Tract Neoplasms [MESH:D001661] (1165) 
 Gallbladder Neoplasms [MESH:D005706] (993)
 Gallbladder Diseases [MESH:D005705] (1215) 
 Gallbladder Neoplasms [MESH:D005706] (993)
 Digestive System Abnormalities [MESH:D004065] (2127) 
 Barrett Esophagus [MESH:D001471] (1930)
 Hirschsprung Disease [MESH:D006627] (361)
 Digestive System Neoplasms [MESH:D004067] (7493) 
 Biliary Tract Neoplasms [MESH:D001661] (1165) 
 Gallbladder Neoplasms [MESH:D005706] (993)
 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) 
 Cecal Neoplasms [MESH:D002430] (822)
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Turcot syndrome [MESH:C536928] (159)
 Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)
 Rectal Neoplasms [MESH:D012004] (717)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Liver Neoplasms [MESH:D008113] (6048) 
 Adenoma, Liver Cell [MESH:D018248] (685)
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Pancreatic cancer, adult [MESH:C535836] (572)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Gastrointestinal Diseases [MESH:D005767] (7443) 
 Esophageal Diseases [MESH:D004935] (4255) 
 Barrett Esophagus [MESH:D001471] (1930)
 Esophageal Stenosis [MESH:D004940] (490)
 Esophagitis [MESH:D004941] (1120)
 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) 
 Appendicitis [MESH:D001064] (774)
 Esophagitis [MESH:D004941] (1120)
 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) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Crohn Disease [MESH:D003424] (2585)
 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) 
 Cecal Neoplasms [MESH:D002430] (822)
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Turcot syndrome [MESH:C536928] (159)
 Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)
 Rectal Neoplasms [MESH:D012004] (717)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Intestinal Diseases [MESH:D007410] (6206) 
 Cecal Diseases [MESH:D002429] (1330) 
 Appendicitis [MESH:D001064] (774)
 Cecal Neoplasms [MESH:D002430] (822)
 Colonic Diseases [MESH:D003108] (5564) 
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Colorectal Neoplasms [MESH:D015179] (5282) 
 Turcot syndrome [MESH:C536928] (159)
 Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Megacolon [MESH:D008531] (386) 
 Hirschsprung Disease [MESH:D006627] (361)
 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) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Crohn Disease [MESH:D003424] (2585)
 Intestinal Neoplasms [MESH:D007414] (5359) 
 Cecal Neoplasms [MESH:D002430] (822)
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Turcot syndrome [MESH:C536928] (159)
 Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)
 Rectal Neoplasms [MESH:D012004] (717)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Intestinal Polyposis [MESH:D044483] (1610) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Malabsorption Syndromes [MESH:D008286] (492) 
 Celiac Disease [MESH:D002446] (340)
 Rectal Diseases [MESH:D012002] (4596) 
 Colorectal Neoplasms [MESH:D015179] (4534) 
 Turcot syndrome [MESH:C536928] (159)
 Rectal Neoplasms [MESH:D012004] (717)
 Peptic Ulcer [MESH:D010437] (3172) 
 Duodenal Ulcer [MESH:D004381] (1549)
 Stomach Ulcer [MESH:D013276] (2915)
 Stomach Diseases [MESH:D013272] (5325) 
 Gastroparesis [MESH:D018589] (732)
 Stomach Neoplasms [MESH:D013274] (4942)
 Gastritis [MESH:D005756] (967) 
 Gastritis, Atrophic [MESH:D005757] (947)
 Peptic Ulcer [MESH:D010437] (2994) 
 Stomach Ulcer [MESH:D013276] (2915)
 Liver Diseases [MESH:D008107] (8167) 
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Hepatomegaly [MESH:D006529] (1169)
 Hepatorenal Syndrome [MESH:D006530] (910)
 Liver Diseases, Parasitic [MESH:D008109] (1009)
 Zellweger Syndrome [MESH:D015211] (182)
 Cholestasis, Intrahepatic [MESH:D002780] (1510) 
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 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)
 Hepatitis, Viral, Human [MESH:D006525] (1766) 
 Hepatitis B [MESH:D006509] (976)
 Hepatitis C [MESH:D006526] (1627)
 Liver Cirrhosis [MESH:D008103] (5542) 
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 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) 
 Adenoma, Liver Cell [MESH:D018248] (685)
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Pancreatic Diseases [MESH:D010182] (4453) 
 Cystic Fibrosis [MESH:D003550] (760)
 Pancreatitis [MESH:D010195] (1924)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Pancreatic cancer, adult [MESH:C535836] (572)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Peritoneal Diseases [MESH:D010532] (1119) 
 Peritoneal Fibrosis [MESH:D056627] (488)
 Peritonitis [MESH:D010538] (800)
C07. Stomatognathic Diseases 
C07. Stomatognathic Diseases
 Stomatognathic Diseases [MESH:D009057] (5348) 
 Jaw Diseases [MESH:D007571] (1608) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330) 
 PCI 5002 [MESH:C568608] (527)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Mouth Diseases [MESH:D009059] (4783) 
 Behcet Syndrome [MESH:D001528] (1784)
 Mucositis [MESH:D052016] (1238)
 Oral Submucous Fibrosis [MESH:D009914] (2432)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Palate [MESH:D002972] (1330) 
 Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)
 Mouth Neoplasms [MESH:D009062] (2263) 
 Leukoplakia, Oral [MESH:D007972] (921)
 Salivary Gland Neoplasms [MESH:D012468] (968) 
 Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)
 Tongue Neoplasms [MESH:D014062] (1518) 
 Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)
 Salivary Gland Diseases [MESH:D012466] (1213) 
 Salivary Gland Neoplasms [MESH:D012468] (968) 
 Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)
 Stomatitis [MESH:D013280] (1235) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Tongue Diseases [MESH:D014060] (1544) 
 Tongue Neoplasms [MESH:D014062] (1518) 
 Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)
 Pharyngeal Diseases [MESH:D010608] (1562) 
 Nasopharyngeal Diseases [MESH:D009302] (1508) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500) 
 Nasopharyngeal carcinoma [MESH:C538339] (1198)
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500) 
 Nasopharyngeal carcinoma [MESH:C538339] (1198)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330) 
 Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Palate [MESH:D002972] (1330) 
 Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)
 Tooth Abnormalities [MESH:D014071] (622) 
 Tooth Agenesis, Selective, 6 [MESH:C567755] (154)
 Tooth Diseases [MESH:D014076] (742) 
 Tooth Abnormalities [MESH:D014071] (622) 
 Tooth Agenesis, Selective, 6 [MESH:C567755] (154)
C08. Respiratory Tract Diseases 
C08. Respiratory Tract Diseases
 Z. Exceptions (1984) 
 Not Fully Specified [NFS] (1984)
 Respiratory Tract Diseases [MESH:D012140] (7881) 
 Ciliary Motility Disorders [MESH:D002925] (104)
 Granuloma, Respiratory Tract [MESH:D015769] (502)
 Bronchial Diseases [MESH:D001982] (4382) 
 Bronchial Hyperreactivity [MESH:D016535] (1357)
 Bronchiectasis [MESH:D001987] (1792)
 Asthma [MESH:D001249] (4098) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 Bronchitis [MESH:D001991] (993) 
 Bronchiolitis [MESH:D001988] (617) 
 Bronchiolitis Obliterans [MESH:D001989] (611)
 Lung Diseases [MESH:D008171] (7249) 
 Cystic Fibrosis [MESH:D003550] (760)
 Hypertension, Pulmonary [MESH:D006976] (2000)
 Pneumonia [MESH:D011014] (3482)
 Pulmonary Edema [MESH:D011654] (2109)
 Pulmonary Embolism [MESH:D011655] (1118)
 Pulmonary Fibrosis [MESH:D011658] (3140)
 Respiratory Distress Syndrome, Adult [MESH:D012128] (864)
 Lung Diseases, Interstitial [MESH:D017563] (2966) 
 Alveolitis, Extrinsic Allergic [MESH:D000542] (496)
 Pneumoconiosis [MESH:D011009] (2789) 
 Anthracosis [MESH:D055008] (1805)
 Asbestosis [MESH:D001195] (935)
 Berylliosis [MESH:D001607] (2005)
 Silicosis [MESH:D012829] (1273)
 Lung Diseases, Obstructive [MESH:D008173] (4697) 
 Asthma [MESH:D001249] (3903)
 Bronchitis [MESH:D001991] (993) 
 Bronchiolitis [MESH:D001988] (617) 
 Bronchiolitis Obliterans [MESH:D001989] (611)
 Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564) 
 Pulmonary Emphysema [MESH:D011656] (1259)
 Lung Injury [MESH:D055370] (3688) 
 Acute Lung Injury [MESH:D055371] (1907)
 Pneumoconiosis [MESH:D011009] (2789) 
 Anthracosis [MESH:D055008] (1805)
 Asbestosis [MESH:D001195] (935)
 Berylliosis [MESH:D001607] (2005)
 Silicosis [MESH:D012829] (1273)
 Ventilator-Induced Lung Injury [MESH:D055397] (1023) 
 Bronchopulmonary Dysplasia [MESH:D001997] (1021)
 Lung Neoplasms [MESH:D008175] (6012) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Small Cell Lung Carcinoma [MESH:D055752] (1380)
 Nose Diseases [MESH:D009668] (1504) 
 Rhinitis [MESH:D012220] (1134) 
 Rhinitis, Allergic, Perennial [MESH:D012221] (625)
 Pleural Diseases [MESH:D010995] (2240) 
 Pleurisy [MESH:D010998] (2070)
 Respiration Disorders [MESH:D012120] (2218) 
 Dyspnea [MESH:D004417] (248)
 Respiratory Distress Syndrome, Adult [MESH:D012128] (864)
 Apnea [MESH:D001049] (748) 
 Sleep Apnea Syndromes [MESH:D012891] (570) 
 Sleep Apnea, Central [MESH:D020182] (347) 
 Congenital central hypoventilation syndrome [MESH:C536209] (341)
 Hyperventilation [MESH:D006985] (654) 
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Respiratory Insufficiency [MESH:D012131] (841) 
 Hypoventilation [MESH:D007040] (360) 
 Congenital central hypoventilation syndrome [MESH:C536209] (341)
 Respiratory Hypersensitivity [MESH:D012130] (4401) 
 Alveolitis, Extrinsic Allergic [MESH:D000542] (495)
 Rhinitis, Allergic, Perennial [MESH:D012221] (625)
 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)
 Legionellosis [MESH:D007876] (612) 
 Legionnaires' Disease [MESH:D007877] (611)
 Respiratory Tract Neoplasms [MESH:D012142] (6053) 
 Lung Neoplasms [MESH:D008175] (6013) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Bronchial Neoplasms [MESH:D001984] (3608) 
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Small Cell Lung Carcinoma [MESH:D055752] (1380)
C09. Otorhinolaryngologic Diseases 
C09. Otorhinolaryngologic Diseases
 Otorhinolaryngologic Diseases [MESH:D010038] (3827) 
 Ciliary Motility Disorders [MESH:D002925] (104)
 Ear Diseases [MESH:D004427] (2522) 
 Hearing Disorders [MESH:D006311] (2103) 
 Hearing Loss [MESH:D034381] (2068)
 Nose Diseases [MESH:D009668] (1504) 
 Rhinitis [MESH:D012220] (1134) 
 Rhinitis, Allergic, Perennial [MESH:D012221] (625)
 Otorhinolaryngologic Neoplasms [MESH:D010039] (1561) 
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500) 
 Nasopharyngeal carcinoma [MESH:C538339] (1198)
 Pharyngeal Diseases [MESH:D010608] (1605) 
 Nasopharyngeal Diseases [MESH:D009302] (1508) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500) 
 Nasopharyngeal carcinoma [MESH:C538339] (1198)
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500) 
 Nasopharyngeal carcinoma [MESH:C538339] (1198)
C10. Nervous System Diseases 
C10. Nervous System Diseases
 Z. Exceptions (4027) 
 Not Fully Specified [NFS] (4027)
 Nervous System Diseases [MESH:D009422] (13325) 
 Chronobiology Disorders [MESH:D021081] (970)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Central Nervous System Diseases [MESH:D002493] (9745) 
 Brain Diseases [MESH:D001927] (9294) 
 Brain Injuries [MESH:D001930] (3429)
 Basal Ganglia Diseases [MESH:D001480] (4268) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Huntington Disease [MESH:D006816] (540)
 Parkinsonian Disorders [MESH:D020734] (4009) 
 Lewy Body Disease [MESH:D020961] (1143)
 Parkinson Disease [MESH:D010300] (3595)
 Brain Diseases, Metabolic [MESH:D001928] (3351) 
 Glutaric aciduria 1 [MESH:C536833] (26)
 Hepatic Encephalopathy [MESH:D006501] (1795)
 Kernicterus [MESH:D007647] (256)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Peroxisomal Disorders [MESH:D018901] (1472) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Zellweger Syndrome [MESH:D015211] (182)
 Refsum Disease [MESH:D012035] (173) 
 Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Brain Neoplasms [MESH:D001932] (2764) 
 Turcot syndrome [MESH:C536928] (159)
 Cerebral Ventricle Neoplasms [MESH:D002551] (772) 
 Choroid Plexus Neoplasms [MESH:D016545] (771) 
 Papilloma, Choroid Plexus [MESH:D020288] (769)
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Cerebellar Diseases [MESH:D002526] (736) 
 Joubert syndrome 1 [MESH:C536293] (20)
 Cerebrovascular Disorders [MESH:D002561] (5542) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Vasospasm, Intracranial [MESH:D020301] (324)
 Brain Ischemia [MESH:D002545] (4873) 
 Ischemic Attack, Transient [MESH:D002546] (1313)
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Carotid Artery Diseases [MESH:D002340] (1993) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Cerebral Small Vessel Diseases [MESH:D059345] (1292) 
 MELAS Syndrome [MESH:D017241] (1061)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Arterial Diseases [MESH:D020765] (2463) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Embolism and Thrombosis [MESH:D002542] (490) 
 Intracranial Thrombosis [MESH:D020767] (481)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (221) 
 Hematoma, Subdural [MESH:D006408] (212)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Dementia [MESH:D003704] (4498) 
 Alzheimer Disease [MESH:D000544] (4275)
 Huntington Disease [MESH:D006816] (540)
 Lewy Body Disease [MESH:D020961] (1143)
 Frontotemporal Lobar Degeneration [MESH:D057174] (310) 
 Frontotemporal Dementia [MESH:D057180] (300)
 Encephalitis [MESH:D004660] (226) 
 Meningoencephalitis [MESH:D008590] (179)
 Epilepsy [MESH:D004827] (6274) 
 Seizures [MESH:D012640] (4502)
 Status Epilepticus [MESH:D013226] (4014)
 Epilepsies, Myoclonic [MESH:D004831] (1344) 
 Myoclonic Epilepsies, Progressive [MESH:D020191] (1101) 
 MERRF Syndrome [MESH:D017243] (1053)
 Epilepsies, Partial [MESH:D004828] (1267) 
 Epilepsy, Temporal Lobe [MESH:D004833] (1108)
 Epilepsy, Generalized [MESH:D004829] (1431) 
 Spasms, Infantile [MESH:D013036] (468)
 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)
 Hypopituitarism [MESH:D007018] (732) 
 Dwarfism, Pituitary [MESH:D004393] (235) 
 Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)
 Leukoencephalopathies [MESH:D056784] (1916) 
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Central Nervous System Infections [MESH:D002494] (1823) 
 Meningoencephalitis [MESH:D008590] (207)
 Central Nervous System Viral Diseases [MESH:D020805] (1416) 
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Encephalitis [MESH:D004660] (351) 
 Meningoencephalitis [MESH:D008590] (179)
 Meningitis [MESH:D008581] (1506) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Meningoencephalitis [MESH:D008590] (179)
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Prion Diseases [MESH:D017096] (488) 
 Scrapie [MESH:D012608] (462)
 Meningitis [MESH:D008581] (352) 
 Meningoencephalitis [MESH:D008590] (179)
 Movement Disorders [MESH:D009069] (4823) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Dyskinesias [MESH:D020820] (1827) 
 Chorea [MESH:D002819] (651) 
 Huntington Disease [MESH:D006816] (540)
 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)
 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)
 Optic Nerve Diseases [MESH:D009901] (1375) 
 Optic Atrophy [MESH:D009896] (1203) 
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Demyelinating Diseases [MESH:D003711] (2917) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Nervous System Malformations [MESH:D009421] (3354) 
 Neural Tube Defects [MESH:D009436] (2143)
 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) 
 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)
 Tuberous Sclerosis [MESH:D014402] (635)
 Nervous System Neoplasms [MESH:D009423] (3073) 
 Melanoma astrocytoma syndrome [MESH:C536149] (159)
 Central Nervous System Neoplasms [MESH:D016543] (3055) 
 Brain Neoplasms [MESH:D001932] (2764) 
 Turcot syndrome [MESH:C536928] (159)
 Cerebral Ventricle Neoplasms [MESH:D002551] (772) 
 Choroid Plexus Neoplasms [MESH:D016545] (771) 
 Papilloma, Choroid Plexus [MESH:D020288] (769)
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Meningeal Neoplasms [MESH:D008577] (984) 
 Meningioma [MESH:D008579] (978)
 Peripheral Nervous System Neoplasms [MESH:D010524] (287) 
 Nerve Sheath Neoplasms [MESH:D018317] (286)
 Neurocutaneous Syndromes [MESH:D020752] (1230) 
 Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)
 Tuberous Sclerosis [MESH:D014402] (635)
 von Hippel-Lindau Disease [MESH:D006623] (580)
 Neurodegenerative Diseases [MESH:D019636] (6613) 
 Lewy Body Disease [MESH:D020961] (1143)
 Parkinson Disease [MESH:D010300] (3595)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Huntington Disease [MESH:D006816] (540)
 Tuberous Sclerosis [MESH:D014402] (635)
 Cockayne Syndrome [MESH:D003057] (107) 
 Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 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)
 Myotonia Congenita [MESH:D009224] (79) 
 Brody myopathy [MESH:C536607] (40)
 Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026) 
 Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Motor Neuron Disease [MESH:D016472] (3670) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Prion Diseases [MESH:D017096] (475) 
 Scrapie [MESH:D012608] (462)
 Tauopathies [MESH:D024801] (4289) 
 Alzheimer Disease [MESH:D000544] (4275)
 TDP-43 Proteinopathies [MESH:D057177] (3337) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Frontotemporal Lobar Degeneration [MESH:D057174] (308) 
 Frontotemporal Dementia [MESH:D057180] (298)
 Neurologic Manifestations [MESH:D009461] (8964) 
 Gait Disorders, Neurologic [MESH:D020233] (491)
 Meningism [MESH:D008580] (43)
 Neurogenic Inflammation [MESH:D020078] (2246)
 Paresis [MESH:D010291] (419)
 Seizures [MESH:D012640] (4514)
 Dyskinesias [MESH:D020820] (3365) 
 Ataxia [MESH:D001259] (1138)
 Catalepsy [MESH:D002375] (1429)
 Hyperkinesis [MESH:D006948] (1799)
 Neurobehavioral Manifestations [MESH:D019954] (5230) 
 Lethargy [MESH:D053609] (1035)
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Language Disorders [MESH:D007806] (653) 
 Speech Disorders [MESH:D013064] (482) 
 Aphasia [MESH:D001037] (219)
 Articulation Disorders [MESH:D001184] (164) 
 Dysarthria [MESH:D004401] (163)
 Confusion [MESH:D003221] (284) 
 Delirium [MESH:D003693] (173)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Intellectual Disability [MESH:D008607] (3054) 
 MORM syndrome [MESH:C536984] (15)
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Down Syndrome [MESH:D004314] (1287)
 Mental Retardation, X-Linked [MESH:D038901] (1854) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Fragile X Syndrome [MESH:D005600] (353)
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Perceptual Disorders [MESH:D010468] (343) 
 Hallucinations [MESH:D006212] (251)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Fasciculation [MESH:D005207] (204)
 Muscle Cramp [MESH:D009120] (135)
 Muscular Atrophy [MESH:D009133] (1234)
 Muscle Weakness [MESH:D018908] (478) 
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 Pain [MESH:D010146] (3875) 
 Headache [MESH:D006261] (1416)
 Neuralgia [MESH:D009437] (2074)
 Back Pain [MESH:D001416] (287) 
 Low Back Pain [MESH:D017116] (244)
 Paralysis [MESH:D010243] (2043) 
 Ophthalmoplegia [MESH:D009886] (1468) 
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)
 Sensation Disorders [MESH:D012678] (5011) 
 Hearing Disorders [MESH:D006311] (2103) 
 Hearing Loss [MESH:D034381] (2068)
 Somatosensory Disorders [MESH:D020886] (4000) 
 Hyperalgesia [MESH:D006930] (3929)
 Paresthesia [MESH:D010292] (416)
 Vision Disorders [MESH:D014786] (501) 
 Photophobia [MESH:D020795] (36)
 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 Diseases [MESH:D009135] (3538) 
 Muscular Disorders, Atrophic [MESH:D020966] (1594) 
 Muscular Dystrophies [MESH:D009136] (1589) 
 Bethlem myopathy [MESH:C535436] (108)
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Muscular Dystrophy, Duchenne [MESH:D020388] (942)
 Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
 Mitochondrial Myopathies [MESH:D017240] (2176) 
 Mitochondrial Encephalomyopathies [MESH:D017237] (1121) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Myopathies, Structural, Congenital [MESH:D020914] (272) 
 Myosclerosis, Autosomal Recessive [MESH:C564968] (45)
 Myositis [MESH:D009220] (2069) 
 Dermatomyositis [MESH:D003882] (1826)
 Polymyositis [MESH:D017285] (2007) 
 Dermatomyositis [MESH:D003882] (1826)
 Myotonic Disorders [MESH:D020967] (138) 
 Myotonia Congenita [MESH:D009224] (79) 
 Brody myopathy [MESH:C536607] (40)
 Peripheral Nervous System Diseases [MESH:D010523] (6151) 
 Diabetic Neuropathies [MESH:D003929] (2442)
 Neuralgia [MESH:D009437] (2078)
 Mononeuropathies [MESH:D020422] (604) 
 Sciatic Neuropathy [MESH:D020426] (477)
 Peripheral Nervous System Neoplasms [MESH:D010524] (287) 
 Nerve Sheath Neoplasms [MESH:D018317] (286)
 Polyneuropathies [MESH:D011115] (1134) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 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 Deprivation [MESH:D012892] (233)
 Sleep Disorders, Intrinsic [MESH:D020919] (1270) 
 Sleep Apnea Syndromes [MESH:D012891] (570) 
 Sleep Apnea, Central [MESH:D020182] (347) 
 Congenital central hypoventilation syndrome [MESH:C536209] (341)
 Trauma, Nervous System [MESH:D020196] (3997) 
 Spinal Cord Injuries [MESH:D013119] (1676)
 Craniocerebral Trauma [MESH:D006259] (3507) 
 Brain Injuries [MESH:D001930] (3431)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (221) 
 Hematoma, Subdural [MESH:D006408] (212)
C11. Eye Diseases 
C11. Eye Diseases
 Eye Diseases [MESH:D005128] (6245) 
 MORM syndrome [MESH:C536984] (15)
 Eyelid Diseases [MESH:D005141] (882)
 Corneal Diseases [MESH:D003316] (1445) 
 Corneal Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)
 Corneal Opacity [MESH:D003318] (544) 
 Peters anomaly [MESH:C537884] (465)
 Eye Abnormalities [MESH:D005124] (1233) 
 Joubert syndrome 1 [MESH:C536293] (20)
 Peters anomaly [MESH:C537884] (465)
 Eye Diseases, Hereditary [MESH:D015785] (1869) 
 Corneal Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Eye Neoplasms [MESH:D005134] (413) 
 Retinal Neoplasms [MESH:D019572] (320) 
 Retinoblastoma [MESH:D012175] (319)
 Lacrimal Apparatus Diseases [MESH:D007766] (644) 
 Dry Eye Syndromes [MESH:D015352] (533)
 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)
 Optic Nerve Diseases [MESH:D009901] (1377) 
 Optic Atrophy [MESH:D009896] (1203) 
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Orbital Diseases [MESH:D009916] (317) 
 Exophthalmos [MESH:D005094] (297)
 Retinal Diseases [MESH:D012164] (3747) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Retinal Detachment [MESH:D012163] (1639)
 Retinal Vein Occlusion [MESH:D012170] (607)
 Retinal Degeneration [MESH:D012162] (2386) 
 Macular Degeneration [MESH:D008268] (995) 
 Fundus Dystrophy, Pseudoinflammatory, Of Sorsby [MESH:C564992] (121)
 Retinal Dystrophies [MESH:D058499] (1315) 
 Retinitis Pigmentosa [MESH:D012174] (1307) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Retinal Neoplasms [MESH:D019572] (320) 
 Retinoblastoma [MESH:D012175] (319)
 Uveal Diseases [MESH:D014603] (2428) 
 Uveitis [MESH:D014605] (2157) 
 Panuveitis [MESH:D015864] (1805) 
 Uveitis, Anterior [MESH:D014606] (1791) 
 Behcet Syndrome [MESH:D001528] (1784)
 Vision Disorders [MESH:D014786] (534) 
 Photophobia [MESH:D020795] (36)
C12. Male Urogenital Diseases 
C12. Male Urogenital Diseases
 Male Urogenital Diseases [MESH:D052801] (8891) 
 Genital Diseases, Male [MESH:D005832] (6794) 
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Neoplasms [MESH:D011471] (6135)
 Infertility [MESH:D007246] (2909) 
 Infertility, Male [MESH:D007248] (2851) 
 Asthenozoospermia [MESH:D053627] (298)
 Azoospermia [MESH:D053713] (1052)
 Penile Diseases [MESH:D010409] (1805) 
 MORM syndrome [MESH:C536984] (15)
 Hypospadias [MESH:D007021] (798)
 Penile Induration [MESH:D010411] (495)
 Penile Neoplasms [MESH:D010412] (890)
 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)
 Urogenital Abnormalities [MESH:D014564] (2065) 
 Allanson Pantzar McLeod syndrome [MESH:C537048] (503)
 Hypospadias [MESH:D007021] (798)
 Urogenital Neoplasms [MESH:D014565] (6932) 
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Penile Neoplasms [MESH:D010412] (890)
 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)
 Wilms Tumor [MESH:D009396] (553)
 Urologic Diseases [MESH:D014570] (7792) 
 Kidney Diseases [MESH:D007674] (7242) 
 Hereditary renal agenesis [MESH:C536482] (89)
 Anuria [MESH:D001002] (833)
 Diabetic Nephropathies [MESH:D003928] (2301)
 Fanconi Syndrome [MESH:D005198] (253)
 Hepatorenal Syndrome [MESH:D006530] (910)
 Hydronephrosis [MESH:D006869] (956)
 Hyperoxaluria [MESH:D006959] (1498)
 Kidney Papillary Necrosis [MESH:D007681] (46)
 Nephrocalcinosis [MESH:D009397] (311)
 Zellweger Syndrome [MESH:D015211] (182)
 Kidney Diseases, Cystic [MESH:D052177] (1009) 
 Joubert syndrome 1 [MESH:C536293] (20)
 Polycystic Kidney Diseases [MESH:D007690] (853) 
 Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)
 Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Wilms Tumor [MESH:D009396] (553)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758) 
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)
 Nephritis, Interstitial [MESH:D009395] (1927) 
 Balkan Nephropathy [MESH:D001449] (772)
 Nephrosis [MESH:D009401] (2228) 
 Nephrotic Syndrome [MESH:D009404] (1536)
 Renal Insufficiency [MESH:D051437] (4951) 
 Acute Kidney Injury [MESH:D058186] (4142) 
 Kidney Tubular Necrosis, Acute [MESH:D007683] (974)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058) 
 Hypomagnesemia 4, Renal [MESH:C567127] (225)
 Bartter Syndrome [MESH:D001477] (241)
 Fanconi Syndrome [MESH:D005198] (253)
 Liddle Syndrome [MESH:D056929] (200)
 Uremia [MESH:D014511] (2898) 
 Azotemia [MESH:D053099] (326)
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 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)
 Cystitis [MESH:D003556] (604) 
 Cystitis, Interstitial [MESH:D018856] (264)
 Urination Disorders [MESH:D014555] (3598) 
 Anuria [MESH:D001002] (833)
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
C13. Female Urogenital Diseases and Pregnancy Complications 
C13. Female Urogenital Diseases and Pregnancy Complications
 Z. Exceptions (1116) 
 Not Fully Specified [NFS] (1116)
 Female Urogenital Diseases [MESH:D052776] (8724) 
 Genital Diseases, Female [MESH:D005831] (5563) 
 Endometriosis [MESH:D004715] (2461)
 Adnexal Diseases [MESH:D000291] (4273) 
 Ovarian Diseases [MESH:D010049] (4255) 
 Ovarian Cysts [MESH:D010048] (2534) 
 Polycystic Ovary Syndrome [MESH:D011085] (2186)
 Ovarian Neoplasms [MESH:D010051] (3281) 
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 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 Cervical Diseases [MESH:D002577] (988) 
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Uterine Neoplasms [MESH:D014594] (2430) 
 Endometrial Neoplasms [MESH:D016889] (1984)
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Vulvar Diseases [MESH:D014845] (873) 
 Vulvar Lichen Sclerosus [MESH:D007724] (825)
 Urogenital Abnormalities [MESH:D014564] (2043) 
 Allanson Pantzar McLeod syndrome [MESH:C537048] (503)
 Hypospadias [MESH:D007021] (798)
 Urogenital Neoplasms [MESH:D014565] (5792) 
 Genital Neoplasms, Female [MESH:D005833] (3810) 
 Ovarian Neoplasms [MESH:D010051] (3281) 
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 Uterine Neoplasms [MESH:D014594] (2433) 
 Endometrial Neoplasms [MESH:D016889] (1989)
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Ureteral Neoplasms [MESH:D014516] (574)
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Wilms Tumor [MESH:D009396] (553)
 Urologic Diseases [MESH:D014570] (7793) 
 Kidney Diseases [MESH:D007674] (7242) 
 Hereditary renal agenesis [MESH:C536482] (89)
 Anuria [MESH:D001002] (833)
 Diabetic Nephropathies [MESH:D003928] (2301)
 Fanconi Syndrome [MESH:D005198] (253)
 Hepatorenal Syndrome [MESH:D006530] (910)
 Hydronephrosis [MESH:D006869] (956)
 Hyperoxaluria [MESH:D006959] (1498)
 Kidney Papillary Necrosis [MESH:D007681] (46)
 Nephrocalcinosis [MESH:D009397] (311)
 Zellweger Syndrome [MESH:D015211] (182)
 Kidney Diseases, Cystic [MESH:D052177] (1009) 
 Joubert syndrome 1 [MESH:C536293] (20)
 Polycystic Kidney Diseases [MESH:D007690] (853) 
 Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)
 Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Wilms Tumor [MESH:D009396] (553)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758) 
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)
 Nephritis, Interstitial [MESH:D009395] (1927) 
 Balkan Nephropathy [MESH:D001449] (772)
 Nephrosis [MESH:D009401] (2228) 
 Nephrotic Syndrome [MESH:D009404] (1536)
 Renal Insufficiency [MESH:D051437] (4951) 
 Acute Kidney Injury [MESH:D058186] (4142) 
 Kidney Tubular Necrosis, Acute [MESH:D007683] (974)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058) 
 Hypomagnesemia 4, Renal [MESH:C567127] (225)
 Bartter Syndrome [MESH:D001477] (241)
 Fanconi Syndrome [MESH:D005198] (253)
 Liddle Syndrome [MESH:D056929] (200)
 Uremia [MESH:D014511] (2898) 
 Azotemia [MESH:D053099] (326)
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 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)
 Cystitis [MESH:D003556] (604) 
 Cystitis, Interstitial [MESH:D018856] (264)
 Urination Disorders [MESH:D014555] (3598) 
 Anuria [MESH:D001002] (833)
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
 Pregnancy Complications [MESH:D011248] (4768) 
 Abortion, Spontaneous [MESH:D000022] (2780)
 Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)
 Prenatal Injuries [MESH:D049188] (1314)
 Fetal Diseases [MESH:D005315] (1206) 
 Chorioamnionitis [MESH:D002821] (313)
 Fetal Growth Retardation [MESH:D005317] (986)
 Hypertension, Pregnancy-Induced [MESH:D046110] (1453) 
 Pre-Eclampsia [MESH:D011225] (1435)
 Obstetric Labor Complications [MESH:D007744] (1550) 
 Obstetric Labor, Premature [MESH:D007752] (1316)
 Fetal Membranes, Premature Rupture [MESH:D005322] (356) 
 Chorioamnionitis [MESH:D002821] (313)
 Placenta Diseases [MESH:D010922] (1781) 
 Chorioamnionitis [MESH:D002821] (313)
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)
 Coronary Vessel Anomalies [MESH:D003330] (317)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Vascular Malformations [MESH:D054079] (1098) 
 Arteriovenous Malformations [MESH:D001165] (1058) 
 Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62)
 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) 
 Cardiac Tamponade [MESH:D002305] (175)
 Heart Arrest [MESH:D006323] (1926)
 Heart Failure [MESH:D006333] (4058)
 Pericardial Effusion [MESH:D010490] (1015)
 Arrhythmias, Cardiac [MESH:D001145] (4679) 
 Tachycardia [MESH:D013610] (3339)
 Cardiomegaly [MESH:D006332] (4081) 
 Cardiomyopathy, Dilated [MESH:D002311] (1576)
 Hypertrophy, Left Ventricular [MESH:D017379] (1430)
 Cardiomyopathies [MESH:D009202] (5331) 
 Cardiomyopathy, Dilated [MESH:D002311] (1576)
 Diabetic Cardiomyopathies [MESH:D058065] (1995)
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Myocarditis [MESH:D009205] (1708)
 Cardiomyopathy, Hypertrophic [MESH:D002312] (1516) 
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 Heart Defects, Congenital [MESH:D006330] (2443) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Coronary Vessel Anomalies [MESH:D003330] (317)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Heart Valve Diseases [MESH:D006349] (3333) 
 Aortic Valve Insufficiency [MESH:D001022] (1002)
 Aortic Valve Stenosis [MESH:D001024] (1742) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Aortic Stenosis, Subvalvular [MESH:D001020] (1455) 
 Cardiomyopathy, Hypertrophic [MESH:D002312] (1451) 
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 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 Thrombosis [MESH:D003328] (255)
 Coronary Stenosis [MESH:D023921] (1806) 
 Coronary Restenosis [MESH:D023903] (1683)
 Myocardial Infarction [MESH:D009203] (4122) 
 Myocardial Stunning [MESH:D017682] (1816)
 Shock, Cardiogenic [MESH:D012770] (269)
 Ventricular Dysfunction [MESH:D018754] (2348) 
 Ventricular Dysfunction, Left [MESH:D018487] (1631)
 Ventricular Outflow Obstruction [MESH:D014694] (976) 
 Aortic Valve Stenosis [MESH:D001024] (810) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Vascular Diseases [MESH:D014652] (8691) 
 Angioedema [MESH:D000799] (837)
 Arteritis [MESH:D001167] (1084)
 Hyperemia [MESH:D006940] (2372)
 Hypotension [MESH:D007022] (4045)
 Retinal Vein Occlusion [MESH:D012170] (607)
 Varicose Veins [MESH:D014648] (383)
 Vascular System Injuries [MESH:D057772] (2086)
 Aneurysm [MESH:D000783] (1886) 
 Aortic Aneurysm [MESH:D001014] (1721) 
 Aortic Aneurysm, Abdominal [MESH:D017544] (1519)
 Angiomatosis [MESH:D000798] (620) 
 von Hippel-Lindau Disease [MESH:D006623] (580)
 Aortic Diseases [MESH:D001018] (1737) 
 Aortic Aneurysm [MESH:D001014] (1721) 
 Aortic Aneurysm, Abdominal [MESH:D017544] (1519)
 Arterial Occlusive Diseases [MESH:D001157] (4520) 
 Arteriosclerosis [MESH:D001161] (4466) 
 Atherosclerosis [MESH:D050197] (4188)
 Coronary Artery Disease [MESH:D003324] (2685)
 Arteriovenous Malformations [MESH:D001165] (1058) 
 Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62)
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Cerebrovascular Disorders [MESH:D002561] (5541) 
 Vasospasm, Intracranial [MESH:D020301] (324)
 Brain Ischemia [MESH:D002545] (4873) 
 Ischemic Attack, Transient [MESH:D002546] (1313)
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Carotid Artery Diseases [MESH:D002340] (1993) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Cerebral Small Vessel Diseases [MESH:D059345] (1292) 
 MELAS Syndrome [MESH:D017241] (1061)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Arterial Diseases [MESH:D020765] (2468) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Intracranial Thrombosis [MESH:D020767] (481)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (221) 
 Hematoma, Subdural [MESH:D006408] (212)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Diabetic Angiopathies [MESH:D003925] (1984) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Embolism and Thrombosis [MESH:D016769] (3374) 
 Embolism [MESH:D004617] (1137) 
 Pulmonary Embolism [MESH:D011655] (1118)
 Embolism, Fat [MESH:D004620] (261) 
 Embolism, Cholesterol [MESH:D017700] (255)
 Thromboembolism [MESH:D013923] (732) 
 Venous Thromboembolism [MESH:D054556] (400)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Intracranial Thrombosis [MESH:D020767] (481)
 Thrombosis [MESH:D013927] (3101) 
 Coronary Thrombosis [MESH:D003328] (255)
 Thromboembolism [MESH:D013923] (732) 
 Venous Thromboembolism [MESH:D054556] (400)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Intracranial Thrombosis [MESH:D020767] (481)
 Venous Thrombosis [MESH:D020246] (1141) 
 Retinal Vein Occlusion [MESH:D012170] (607)
 Hemostatic Disorders [MESH:D020141] (2894) 
 Multiple Myeloma [MESH:D009101] (2765)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Hypertension [MESH:D006973] (5655) 
 Hypertension, Malignant [MESH:D006974] (621)
 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 Thrombosis [MESH:D003328] (255)
 Coronary Stenosis [MESH:D023921] (1806) 
 Coronary Restenosis [MESH:D023903] (1683)
 Myocardial Infarction [MESH:D009203] (4151) 
 Myocardial Stunning [MESH:D017682] (1816)
 No-Reflow Phenomenon [MESH:D054318] (277)
 Shock, Cardiogenic [MESH:D012770] (269)
 Peripheral Vascular Diseases [MESH:D016491] (1412) 
 Raynaud Disease [MESH:D011928] (490)
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Vasculitis [MESH:D014657] (2604) 
 Arteritis [MESH:D001167] (1084)
 Behcet Syndrome [MESH:D001528] (1784)
C15. Hemic and Lymphatic Diseases 
C15. Hemic and Lymphatic Diseases
 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, Hemolytic [MESH:D000743] (3083) 
 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to [MESH:C565557] (312)
 Anemia, Hemolytic, Autoimmune [MESH:D000744] (117)
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Anemia, Hemolytic, Congenital [MESH:D000745] (2001) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Anemia, Hypochromic [MESH:D000747] (616) 
 Anemia, Iron-Deficiency [MESH:D018798] (547)
 Anemia, Macrocytic [MESH:D000748] (382) 
 Anemia, Megaloblastic [MESH:D000749] (288)
 Blood Coagulation Disorders [MESH:D001778] (1828) 
 Thrombocythemia, Essential [MESH:D013920] (707)
 Blood Coagulation Disorders, Inherited [MESH:D025861] (720) 
 Thrombasthenia [MESH:D013915] (98)
 Blood Group Incompatibility [MESH:D001787] (277) 
 Erythroblastosis, Fetal [MESH:D004899] (275) 
 Kernicterus [MESH:D007647] (256)
 Blood Platelet Disorders [MESH:D001791] (3174) 
 Thrombasthenia [MESH:D013915] (98)
 Thrombocytopenia [MESH:D013921] (2966) 
 Thrombocytopenia, Neonatal Alloimmune [MESH:D054098] (79)
 Thrombotic Microangiopathies [MESH:D057049] (2598) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Thrombocytosis [MESH:D013922] (720) 
 Thrombocythemia, Essential [MESH:D013920] (707)
 Blood Protein Disorders [MESH:D001796] (3051) 
 Hypoproteinemia [MESH:D007019] (1335) 
 Hypoalbuminemia [MESH:D034141] (1332)
 Paraproteinemias [MESH:D010265] (2781) 
 Multiple Myeloma [MESH:D009101] (2765)
 Bone Marrow Diseases [MESH:D001855] (2944) 
 Anemia, Aplastic [MESH:D000741] (1925) 
 Anemia, Hypoplastic, Congenital [MESH:D029502] (1665) 
 Fanconi Anemia [MESH:D005199] (1604)
 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)
 Thrombocytosis [MESH:D013922] (720) 
 Thrombocythemia, Essential [MESH:D013920] (707)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Hemorrhagic Disorders [MESH:D006474] (3359) 
 Thrombasthenia [MESH:D013915] (98)
 Thrombocythemia, Essential [MESH:D013920] (707)
 Hemostatic Disorders [MESH:D020141] (2932) 
 Multiple Myeloma [MESH:D009101] (2765)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Leukocyte Disorders [MESH:D007960] (2662) 
 Eosinophilia [MESH:D004802] (537)
 Leukocytosis [MESH:D007964] (988)
 Leukostasis [MESH:D018921] (769)
 Leukopenia [MESH:D007970] (1921) 
 Lymphopenia [MESH:D008231] (990)
 Agranulocytosis [MESH:D000380] (1675) 
 Neutropenia [MESH:D009503] (1629)
 Phagocyte Bactericidal Dysfunction [MESH:D010585] (998) 
 Job Syndrome [MESH:D007589] (772) 
 Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)
 Lymphatic Diseases [MESH:D008206] (5167) 
 Splenic Diseases [MESH:D013158] (1323)
 Thymus Neoplasms [MESH:D013953] (247)
 Histiocytosis [MESH:D015614] (336) 
 Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315) 
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Lymphoproliferative Disorders [MESH:D008232] (4638) 
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Giant Lymph Node Hyperplasia [MESH:D005871] (1013)
 Sarcoidosis [MESH:D012507] (895)
 Leukemia, Lymphoid [MESH:D007945] (3047) 
 Leukemia, T-Cell [MESH:D015458] (395)
 Leukemia, B-Cell [MESH:D015448] (2564) 
 Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
 Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) 
 Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)
 Lymphoma [MESH:D008223] (3684) 
 Hodgkin Disease [MESH:D006689] (1082)
 Lymphoma, Non-Hodgkin [MESH:D008228] (3330) 
 Burkitt Lymphoma [MESH:D002051] (691)
 Lymphoma, Follicular [MESH:D008224] (1025)
 Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)
 Lymphoma, Mantle-Cell [MESH:D020522] (561)
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Burkitt Lymphoma [MESH:D002051] (691)
 Lymphoma, 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) 
 Hereditary renal agenesis [MESH:C536482] (89)
 Abnormalities, Multiple [MESH:D000015] (3192) 
 Ulnar-mammary syndrome [MESH:C536937] (57)
 MORM syndrome [MESH:C536984] (15)
 Bloom Syndrome [MESH:D001816] (107)
 Costello Syndrome [MESH:D056685] (407)
 Down Syndrome [MESH:D004314] (1287)
 Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)
 Zellweger Syndrome [MESH:D015211] (182)
 Cockayne Syndrome [MESH:D003057] (107) 
 Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)
 Ectodermal Dysplasia [MESH:D004476] (938) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Cardiovascular Abnormalities [MESH:D018376] (3294) 
 Heart Defects, Congenital [MESH:D006330] (2611) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Coronary Vessel Anomalies [MESH:D003330] (317)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Vascular Malformations [MESH:D054079] (1108) 
 Arteriovenous Malformations [MESH:D001165] (1058) 
 Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62)
 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) 
 Down Syndrome [MESH:D004314] (1287)
 Sex Chromosome Disorders [MESH:D025064] (479) 
 Fragile X Syndrome [MESH:D005600] (353)
 Digestive System Abnormalities [MESH:D004065] (507) 
 Hirschsprung Disease [MESH:D006627] (361)
 Eye Abnormalities [MESH:D005124] (1233) 
 Joubert syndrome 1 [MESH:C536293] (20)
 Peters anomaly [MESH:C537884] (465)
 Musculoskeletal Abnormalities [MESH:D009139] (3779) 
 Craniofacial Abnormalities [MESH:D019465] (3064) 
 Microcephaly [MESH:D008831] (700)
 Maxillofacial Abnormalities [MESH:D019767] (1448) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Limb Deformities, Congenital [MESH:D017880] (1813) 
 Acromicric dysplasia [MESH:C535662] (520)
 Nervous System Malformations [MESH:D009421] (3354) 
 Neural Tube Defects [MESH:D009436] (2143)
 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) 
 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)
 Tuberous Sclerosis [MESH:D014402] (635)
 Skin Abnormalities [MESH:D012868] (1723) 
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Epidermolysis Bullosa Simplex [MESH:D016110] (140)
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Ichthyosis [MESH:D007057] (481) 
 Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)
 Xeroderma Pigmentosum [MESH:D014983] (213) 
 Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Tooth Abnormalities [MESH:D014071] (622)
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330)
 Micrognathism [MESH:D008844] (230) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Palate [MESH:D002972] (1330)
 Urogenital Abnormalities [MESH:D014564] (2064) 
 Allanson Pantzar McLeod syndrome [MESH:C537048] (503)
 Hypospadias [MESH:D007021] (798)
 Fetal Diseases [MESH:D005315] (1205) 
 Chorioamnionitis [MESH:D002821] (313)
 Fetal Growth Retardation [MESH:D005317] (986)
 Genetic Diseases, Inborn [MESH:D030342] (9766) 
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Camurati-Engelmann Syndrome [MESH:D003966] (492)
 Costello Syndrome [MESH:D056685] (407)
 Cystic Fibrosis [MESH:D003550] (760)
 Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478)
 Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)
 Anemia, Hemolytic, Congenital [MESH:D000745] (2001) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Anemia, Hypoplastic, Congenital [MESH:D029502] (1665) 
 Fanconi Anemia [MESH:D005199] (1604)
 Blood Coagulation Disorders, Inherited [MESH:D025861] (722) 
 Thrombasthenia [MESH:D013915] (98)
 Chromosome Disorders [MESH:D025063] (2030) 
 Down Syndrome [MESH:D004314] (1287)
 Sex Chromosome Disorders [MESH:D025064] (479) 
 Fragile X Syndrome [MESH:D005600] (353)
 Dwarfism [MESH:D004392] (783) 
 Laron Syndrome [MESH:D046150] (91)
 Cockayne Syndrome [MESH:D003057] (107) 
 Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)
 Eye Diseases, Hereditary [MESH:D015785] (1867) 
 Corneal Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Genetic Diseases, X-Linked [MESH:D040181] (3028) 
 Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)
 Muscular Dystrophy, Duchenne [MESH:D020388] (942)
 Mental Retardation, X-Linked [MESH:D038901] (1867) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Fragile X Syndrome [MESH:D005600] (353)
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Huntington Disease [MESH:D006816] (540)
 Tuberous Sclerosis [MESH:D014402] (635)
 Cockayne Syndrome [MESH:D003057] (107) 
 Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 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) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Fragile X Syndrome [MESH:D005600] (353)
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Myotonia Congenita [MESH:D009224] (79) 
 Brody myopathy [MESH:C536607] (40)
 Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026) 
 Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Metabolism, Inborn Errors [MESH:D008661] (6032) 
 Trimethylaminuria [MESH:C536561] (61)
 3-Methylglutaconic Aciduria, Type I [MESH:C562801] (29)
 Dihydropyrimidinase Deficiency [MESH:C562815] (27)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565) 
 Glutaric aciduria 1 [MESH:C536833] (26)
 Methylmalonic acidemia [MESH:C537358] (764)
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 Hyperhomocysteinemia [MESH:D020138] (1724)
 Multiple Carboxylase Deficiency [MESH:D009100] (51) 
 Holocarboxylase Synthetase Deficiency [MESH:D028922] (25)
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Peroxisomal Disorders [MESH:D018901] (1472) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Zellweger Syndrome [MESH:D015211] (182)
 Refsum Disease [MESH:D012035] (173) 
 Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Multiple Carboxylase Deficiency [MESH:D009100] (51) 
 Holocarboxylase Synthetase Deficiency [MESH:D028922] (25)
 Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324) 
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Hyperbilirubinemia, Hereditary [MESH:D006933] (476) 
 Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)
 Gilbert Disease [MESH:D005878] (259)
 Crigler-Najjar Syndrome [MESH:D003414] (255) 
 Crigler Najjar syndrome, type 2 [MESH:C536213] (254)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Lipidoses [MESH:D008064] (1655) 
 Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026) 
 Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Lysosomal Storage Diseases [MESH:D016464] (761) 
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Metal Metabolism, Inborn Errors [MESH:D008664] (2017) 
 Hemochromatosis [MESH:D006432] (1694)
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Peroxisomal Disorders [MESH:D018901] (1788) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 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)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027) 
 Hypomagnesemia 4, Renal [MESH:C567127] (225)
 Fanconi Syndrome [MESH:D005198] (253)
 Liddle Syndrome [MESH:D056929] (200)
 Muscular Dystrophies [MESH:D009136] (1597) 
 Bethlem myopathy [MESH:C535436] (108)
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Muscular Dystrophy, Duchenne [MESH:D020388] (942)
 Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
 Neoplastic Syndromes, Hereditary [MESH:D009386] (2578) 
 Turcot syndrome [MESH:C536928] (159)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 Li-Fraumeni Syndrome [MESH:D016864] (859)
 Tuberous Sclerosis [MESH:D014402] (635)
 Wilms Tumor [MESH:D009396] (553)
 Adenomatous Polyposis Coli [MESH:D011125] (1565) 
 Desmoid disease, hereditary [MESH:C535944] (58)
 Multiple Endocrine Neoplasia [MESH:D009377] (375) 
 Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)
 Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)
 Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 Skin Diseases, Genetic [MESH:D012873] (3456) 
 Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)
 Dermatitis, Atopic [MESH:D003876] (2052)
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (259) 
 Epidermolysis Bullosa Simplex [MESH:D016110] (140)
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Xeroderma Pigmentosum [MESH:D014983] (213) 
 Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)
 Infant, Newborn, Diseases [MESH:D007232] (3064) 
 Asphyxia Neonatorum [MESH:D001238] (1648)
 Cystic Fibrosis [MESH:D003550] (760)
 Thrombocytopenia, Neonatal Alloimmune [MESH:D054098] (79)
 Erythroblastosis, Fetal [MESH:D004899] (257) 
 Kernicterus [MESH:D007647] (256)
 Hyperbilirubinemia, Neonatal [MESH:D051556] (469) 
 Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)
 Ichthyosis [MESH:D007057] (476) 
 Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)
 Infant, Premature, Diseases [MESH:D007235] (1292) 
 Bronchopulmonary Dysplasia [MESH:D001997] (1021)
C17. Skin and Connective Tissue Diseases 
C17. Skin and Connective Tissue Diseases
 Connective Tissue Diseases [MESH:D003240] (4490) 
 Dermatomyositis [MESH:D003882] (1826)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317)
 Mixed Connective Tissue Disease [MESH:D008947] (4)
 Penile Induration [MESH:D010411] (495)
 Scleroderma, Localized [MESH:D012594] (1597)
 Collagen Diseases [MESH:D003095] (1267) 
 Keloid [MESH:D007627] (1111)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 Noonan Syndrome [MESH:D009634] (506) 
 Noonan syndrome 3 [MESH:C537847] (118)
 Rheumatic Diseases [MESH:D012216] (3619) 
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Skin Diseases [MESH:D012871] (8774) 
 Dermatomyositis [MESH:D003882] (1826)
 Exanthema [MESH:D005076] (301)
 Pruritus [MESH:D011537] (647)
 Scleroderma, Localized [MESH:D012594] (1597)
 Acneiform Eruptions [MESH:D017486] (1312) 
 Chloracne [MESH:D054506] (1274)
 Breast Diseases [MESH:D001941] (6148) 
 Ulnar-mammary syndrome [MESH:C536937] (57)
 Breast Neoplasms [MESH:D001943] (6077) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 Dermatitis [MESH:D003872] (4530) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Dermatitis, Occupational [MESH:D009783] (311)
 Drug Eruptions [MESH:D003875] (2697) 
 Serum Sickness [MESH:D012713] (484)
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Erythema [MESH:D004890] (1330) 
 Erythema Multiforme [MESH:D004892] (1185) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Facial Dermatoses [MESH:D005148] (1336) 
 Acneiform Eruptions [MESH:D017486] (1312) 
 Chloracne [MESH:D054506] (1274)
 Hair Diseases [MESH:D006201] (1891) 
 Hypotrichosis [MESH:D007039] (1513) 
 Alopecia [MESH:D000505] (1453)
 Keratosis [MESH:D007642] (1941) 
 Ichthyosis [MESH:D007057] (481) 
 Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)
 Photosensitivity Disorders [MESH:D010787] (272) 
 Xeroderma Pigmentosum [MESH:D014983] (213) 
 Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)
 Pigmentation Disorders [MESH:D010859] (1215) 
 Xeroderma Pigmentosum [MESH:D014983] (213) 
 Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)
 Sebaceous Gland Diseases [MESH:D012625] (245) 
 Sebaceous Gland Neoplasms [MESH:D012626] (154)
 Skin Abnormalities [MESH:D012868] (1709) 
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Epidermolysis Bullosa Simplex [MESH:D016110] (140)
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Ichthyosis [MESH:D007057] (481) 
 Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)
 Xeroderma Pigmentosum [MESH:D014983] (213) 
 Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)
 Skin Diseases, Eczematous [MESH:D017443] (3740) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Dermatitis, Occupational [MESH:D009783] (311)
 Skin Diseases, Genetic [MESH:D012873] (3481) 
 Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)
 Dermatitis, Atopic [MESH:D003876] (2052)
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Epidermolysis Bullosa Simplex [MESH:D016110] (140)
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Xeroderma Pigmentosum [MESH:D014983] (213) 
 Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)
 Skin Diseases, Infectious [MESH:D012874] (2684) 
 Skin Diseases, Parasitic [MESH:D012876] (2526) 
 Leishmaniasis [MESH:D007896] (2516) 
 Leishmaniasis, Cutaneous [MESH:D016773] (2359) 
 Leishmaniasis, Mucocutaneous [MESH:D007897] (606)
 Skin Diseases, Metabolic [MESH:D012875] (1574) 
 Lipodystrophy [MESH:D008060] (930) 
 Lipodystrophy, Familial Partial [MESH:D052496] (589)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Skin Diseases, Papulosquamous [MESH:D017444] (3392) 
 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)
 Skin Diseases, Vesiculobullous [MESH:D012872] (1754) 
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Epidermolysis Bullosa Simplex [MESH:D016110] (140)
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Erythema Multiforme [MESH:D004892] (1185) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Skin Neoplasms [MESH:D012878] (2991) 
 Sebaceous Gland Neoplasms [MESH:D012626] (154)
C18. Nutritional and Metabolic Diseases 
C18. Nutritional and Metabolic Diseases
 Metabolic Diseases [MESH:D008659] (9025) 
 Metabolic Syndrome X [MESH:D024821] (2151)
 Acid-Base Imbalance [MESH:D000137] (854) 
 Acidosis [MESH:D000138] (626) 
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 Brain Diseases, Metabolic [MESH:D001928] (3350) 
 Glutaric aciduria 1 [MESH:C536833] (26)
 Hepatic Encephalopathy [MESH:D006501] (1795)
 Kernicterus [MESH:D007647] (256)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Peroxisomal Disorders [MESH:D018901] (1472) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Zellweger Syndrome [MESH:D015211] (182)
 Refsum Disease [MESH:D012035] (173) 
 Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Calcium Metabolism Disorders [MESH:D002128] (3634) 
 Hypercalcemia [MESH:D006934] (1999)
 Calcinosis [MESH:D002114] (2989) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Nephrocalcinosis [MESH:D009397] (311)
 DNA Repair-Deficiency Disorders [MESH:D049914] (2245) 
 Bloom Syndrome [MESH:D001816] (107)
 Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)
 Fanconi Anemia [MESH:D005199] (1604)
 Li-Fraumeni Syndrome [MESH:D016864] (859)
 Cockayne Syndrome [MESH:D003057] (107) 
 Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)
 Xeroderma Pigmentosum [MESH:D014983] (213) 
 Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)
 Glucose Metabolism Disorders [MESH:D044882] (6122) 
 Hypoglycemia [MESH:D007003] (2420)
 Diabetes Mellitus [MESH:D003920] (5891) 
 Diabetes Mellitus, Experimental [MESH:D003921] (4771)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
 Diabetes Mellitus, Type 2 [MESH:D003924] (4219) 
 Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)
 Hyperglycemia [MESH:D006943] (1858) 
 Glucose Intolerance [MESH:D018149] (605)
 Hyperinsulinism [MESH:D006946] (3586) 
 Insulin Resistance [MESH:D007333] (3511) 
 Metabolic Syndrome X [MESH:D024821] (2151)
 Iron Metabolism Disorders [MESH:D019189] (2139) 
 Anemia, Iron-Deficiency [MESH:D018798] (547)
 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)
 Lipodystrophy [MESH:D008060] (930) 
 Lipodystrophy, Familial Partial [MESH:D052496] (589)
 Lipidoses [MESH:D008064] (1655) 
 Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026) 
 Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Malabsorption Syndromes [MESH:D008286] (1869) 
 Celiac Disease [MESH:D002446] (340)
 Hyperhomocysteinemia [MESH:D020138] (1716)
 Metabolism, Inborn Errors [MESH:D008661] (6028) 
 Trimethylaminuria [MESH:C536561] (61)
 3-Methylglutaconic Aciduria, Type I [MESH:C562801] (29)
 Dihydropyrimidinase Deficiency [MESH:C562815] (27)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559) 
 Glutaric aciduria 1 [MESH:C536833] (26)
 Methylmalonic acidemia [MESH:C537358] (764)
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 Hyperhomocysteinemia [MESH:D020138] (1724)
 Multiple Carboxylase Deficiency [MESH:D009100] (51) 
 Holocarboxylase Synthetase Deficiency [MESH:D028922] (25)
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Hepatolenticular Degeneration [MESH:D006527] (473)
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Peroxisomal Disorders [MESH:D018901] (1472) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Zellweger Syndrome [MESH:D015211] (182)
 Refsum Disease [MESH:D012035] (173) 
 Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Multiple Carboxylase Deficiency [MESH:D009100] (51) 
 Holocarboxylase Synthetase Deficiency [MESH:D028922] (25)
 Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324) 
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Hyperbilirubinemia, Hereditary [MESH:D006933] (476) 
 Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)
 Gilbert Disease [MESH:D005878] (259)
 Crigler-Najjar Syndrome [MESH:D003414] (255) 
 Crigler Najjar syndrome, type 2 [MESH:C536213] (254)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Lipidoses [MESH:D008064] (1655) 
 Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026) 
 Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Lysosomal Storage Diseases [MESH:D016464] (761) 
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Mucolipidoses [MESH:D009081] (78) 
 Neuraminidase 1 deficiency [MESH:C537366] (31)
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Niemann-Pick Diseases [MESH:D009542] (136) 
 Niemann-Pick Disease, Type C [MESH:D052556] (103)
 Metal Metabolism, Inborn Errors [MESH:D008664] (2017) 
 Hemochromatosis [MESH:D006432] (1694)
 Hepatolenticular Degeneration [MESH:D006527] (473)
 Peroxisomal Disorders [MESH:D018901] (1788) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 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)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026) 
 Hypomagnesemia 4, Renal [MESH:C567127] (225)
 Fanconi Syndrome [MESH:D005198] (253)
 Liddle Syndrome [MESH:D056929] (200)
 Mitochondrial Diseases [MESH:D028361] (2561) 
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Mitochondrial Myopathies [MESH:D017240] (2176) 
 Mitochondrial Encephalomyopathies [MESH:D017237] (1121) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149) 
 Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Proteostasis Deficiencies [MESH:D057165] (3522) 
 Amyloidosis [MESH:D000686] (791) 
 Amyloidosis, Familial [MESH:D028226] (696) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 Cerebral Amyloid Angiopathy [MESH:D016657] (470) 
 Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377) 
 Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)
 TDP-43 Proteinopathies [MESH:D057177] (3337) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Frontotemporal Lobar Degeneration [MESH:D057174] (308) 
 Frontotemporal Dementia [MESH:D057180] (298)
 Skin Diseases, Metabolic [MESH:D012875] (1574) 
 Lipodystrophy [MESH:D008060] (930) 
 Lipodystrophy, Familial Partial [MESH:D052496] (589)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Wasting Syndrome [MESH:D019282] (1959) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Water-Electrolyte Imbalance [MESH:D014883] (2790) 
 Hypercalcemia [MESH:D006934] (1999)
 Hyperkalemia [MESH:D006947] (485)
 Hyponatremia [MESH:D007010] (789)
 Nutrition Disorders [MESH:D009748] (4945) 
 Malnutrition [MESH:D044342] (2754) 
 Starvation [MESH:D013217] (50)
 Deficiency Diseases [MESH:D003677] (2742) 
 Protein Deficiency [MESH:D011488] (1057)
 Avitaminosis [MESH:D001361] (2304) 
 Vitamin A Deficiency [MESH:D014802] (705)
 Vitamin B Deficiency [MESH:D014804] (1817) 
 Hyperhomocysteinemia [MESH:D020138] (1716)
 Overnutrition [MESH:D044343] (4463) 
 Obesity [MESH:D009765] (4462) 
 MORM syndrome [MESH:C536984] (15)
 Wasting Syndrome [MESH:D019282] (1959) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
C19. Endocrine System Diseases 
C19. Endocrine System Diseases
 Endocrine System Diseases [MESH:D004700] (8062) 
 Bone Diseases, Endocrine [MESH:D001849] (173)
 Adrenal Gland Diseases [MESH:D000307] (2397) 
 Adrenal Cortex Diseases [MESH:D000303] (969) 
 Adrenal Cortex Neoplasms [MESH:D000306] (823) 
 Adrenocortical Carcinoma [MESH:D018268] (821) 
 Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)
 Adrenal Gland Neoplasms [MESH:D000310] (917) 
 Adrenal Cortex Neoplasms [MESH:D000306] (823) 
 Adrenocortical Carcinoma [MESH:D018268] (821) 
 Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)
 Adrenal Insufficiency [MESH:D000309] (1599) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Adrenocortical Hyperfunction [MESH:D000308] (618) 
 Hyperaldosteronism [MESH:D006929] (419) 
 Bartter Syndrome [MESH:D001477] (241)
 Diabetes Mellitus [MESH:D003920] (6159) 
 Diabetes Mellitus, Experimental [MESH:D003921] (4771)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
 Diabetes Complications [MESH:D048909] (4129) 
 Diabetic Cardiomyopathies [MESH:D058065] (1995)
 Diabetic Nephropathies [MESH:D003928] (2301)
 Diabetic Neuropathies [MESH:D003929] (2443)
 Diabetic Angiopathies [MESH:D003925] (1984) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Diabetes Mellitus, Type 2 [MESH:D003924] (4219) 
 Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)
 Dwarfism [MESH:D004392] (698) 
 Laron Syndrome [MESH:D046150] (91)
 Dwarfism, Pituitary [MESH:D004393] (235) 
 Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Pituitary Neoplasms [MESH:D010911] (981)
 Adrenal Gland Neoplasms [MESH:D000310] (917) 
 Adrenal Cortex Neoplasms [MESH:D000306] (823) 
 Adrenocortical Carcinoma [MESH:D018268] (821) 
 Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)
 Multiple Endocrine Neoplasia [MESH:D009377] (375) 
 Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)
 Multiple Endocrine Neoplasia Type 2b [MESH:D018814] (75)
 Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102) 
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Ovarian Neoplasms [MESH:D010051] (3275) 
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Pancreatic cancer, adult [MESH:C535836] (572)
 Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Thyroid Neoplasms [MESH:D013964] (2040) 
 Thyroid cancer, anaplastic [MESH:C536910] (489)
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Thyroid cancer, medullary [MESH:C536914] (74)
 Gonadal Disorders [MESH:D006058] (5088) 
 Puberty, Precocious [MESH:D011629] (1147)
 Ovarian Diseases [MESH:D010049] (4253) 
 Ovarian Cysts [MESH:D010048] (2534) 
 Polycystic Ovary Syndrome [MESH:D011085] (2186)
 Ovarian Neoplasms [MESH:D010051] (3281) 
 Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)
 Parathyroid Diseases [MESH:D010279] (1604) 
 Hyperparathyroidism [MESH:D006961] (1475) 
 Hyperparathyroidism, Secondary [MESH:D006962] (1138)
 Pituitary Diseases [MESH:D010900] (1829) 
 Pituitary Neoplasms [MESH:D010911] (981)
 Hypopituitarism [MESH:D007018] (732) 
 Dwarfism, Pituitary [MESH:D004393] (235) 
 Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)
 Thyroid Diseases [MESH:D013959] (2808) 
 Hyperthyroidism [MESH:D006980] (1191)
 Hyperthyroxinemia [MESH:D006981] (659) 
 Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478)
 Thyroid Neoplasms [MESH:D013964] (2040) 
 Thyroid cancer, anaplastic [MESH:C536910] (489)
 Familial medullary thyroid carcinoma [MESH:C536911] (101)
 Thyroid cancer, medullary [MESH:C536914] (74)
C20. Immune System Diseases 
C20. Immune System Diseases
 Immune System Diseases [MESH:D007154] (7674) 
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Graft vs Host Disease [MESH:D006086] (674)
 Autoimmune Diseases [MESH:D001327] (5067) 
 Anemia, Hemolytic, Autoimmune [MESH:D000744] (117)
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Rheumatoid [MESH:D001172] (3601)
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1893)
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Hepatitis, Autoimmune [MESH:D019693] (1982)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Blood Group Incompatibility [MESH:D001787] (277) 
 Erythroblastosis, Fetal [MESH:D004899] (275) 
 Kernicterus [MESH:D007647] (256)
 Hypersensitivity [MESH:D006967] (5873) 
 Drug Hypersensitivity [MESH:D004342] (4000) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 Drug Eruptions [MESH:D003875] (2695) 
 Serum Sickness [MESH:D012713] (484)
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Hypersensitivity, Delayed [MESH:D006968] (3408) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Hypersensitivity, Immediate [MESH:D006969] (4980) 
 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) 
 Alveolitis, Extrinsic Allergic [MESH:D000542] (495)
 Asthma [MESH:D001249] (3914)
 Rhinitis, Allergic, Perennial [MESH:D012221] (625)
 Urticaria [MESH:D014581] (2668) 
 Angioedema [MESH:D000799] (837)
 Immune Complex Diseases [MESH:D007105] (782) 
 Serum Sickness [MESH:D012713] (484)
 Immunologic Deficiency Syndromes [MESH:D007153] (3788) 
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Lymphopenia [MESH:D008231] (990)
 HIV Infections [MESH:D015658] (3402) 
 Acquired Immunodeficiency Syndrome [MESH:D000163] (743)
 HIV Seropositivity [MESH:D006679] (480)
 HIV Wasting Syndrome [MESH:D019247] (1956)
 AIDS-Related Opportunistic Infections [MESH:D017088] (944) 
 AIDS-related Kaposi sarcoma [MESH:C554498] (914)
 Phagocyte Bactericidal Dysfunction [MESH:D010585] (999) 
 Job Syndrome [MESH:D007589] (772) 
 Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)
 Immunoproliferative Disorders [MESH:D007160] (4761) 
 Lymphoproliferative Disorders [MESH:D008232] (4734) 
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Giant Lymph Node Hyperplasia [MESH:D005871] (1013)
 Multiple Myeloma [MESH:D009101] (2767)
 Leukemia, Lymphoid [MESH:D007945] (3047) 
 Leukemia, T-Cell [MESH:D015458] (395)
 Leukemia, B-Cell [MESH:D015448] (2564) 
 Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
 Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) 
 Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)
 Lymphoma [MESH:D008223] (3684) 
 Hodgkin Disease [MESH:D006689] (1082)
 Lymphoma, Non-Hodgkin [MESH:D008228] (3330) 
 Burkitt Lymphoma [MESH:D002051] (691)
 Lymphoma, Follicular [MESH:D008224] (1025)
 Lymphoma, Mantle-Cell [MESH:D020522] (561)
 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, Large-Cell, Anaplastic [MESH:D017728] (420)
 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)
 Salmonella Infections, Animal [MESH:D012481] (604)
 Sheep Diseases [MESH:D012757] (473) 
 Scrapie [MESH:D012608] (462)
C23. Pathological Conditions, Signs and Symptoms 
C23. Pathological Conditions, Signs and Symptoms
 Pathological Conditions, Anatomical [MESH:D020763] (6074) 
 Alopecia [MESH:D000505] (1383)
 Cysts [MESH:D003560] (133)
 Plaque, Amyloid [MESH:D058225] (334)
 Plaque, Atherosclerotic [MESH:D058226] (696)
 Ventricular Remodeling [MESH:D020257] (686)
 Atrophy [MESH:D001284] (2603) 
 Muscular Atrophy [MESH:D009133] (1234)
 Hernia [MESH:D006547] (2825) 
 Hernia, Diaphragmatic [MESH:D006548] (2647)
 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) 
 Azotemia [MESH:D053099] (326)
 Emphysema [MESH:D004646] (1096)
 Gliosis [MESH:D005911] (1419)
 Hyperplasia [MESH:D006965] (2463)
 Leukocytosis [MESH:D007964] (978)
 Necrosis [MESH:D009336] (4019)
 Neointima [MESH:D058426] (814)
 Nerve Degeneration [MESH:D009410] (4061)
 Ulcer [MESH:D014456] (392)
 Arrhythmias, Cardiac [MESH:D001145] (4658) 
 Tachycardia [MESH:D013610] (3339)
 Chromosome Aberrations [MESH:D002869] (2352) 
 Chromosome Breakage [MESH:D019457] (139)
 Micronuclei, Chromosome-Defective [MESH:D048629] (1013)
 Translocation, Genetic [MESH:D014178] (557)
 Aneuploidy [MESH:D000782] (1237) 
 Monosomy [MESH:D009006] (1121) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Disease Attributes [MESH:D020969] (3654) 
 Disease Progression [MESH:D018450] (2868)
 Recurrence [MESH:D012008] (830)
 Disease Susceptibility [MESH:D004198] (1200) 
 Genetic Predisposition to Disease [MESH:D020022] (966)
 Facies [MESH:D019066] (738) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Fibrosis [MESH:D005355] (3133) 
 Peritoneal Fibrosis [MESH:D056627] (488)
 Cicatrix [MESH:D002921] (1115) 
 Keloid [MESH:D007627] (1110)
 Granuloma [MESH:D006099] (587) 
 Granuloma, Respiratory Tract [MESH:D015769] (502)
 Growth Disorders [MESH:D006130] (2438) 
 Meier-Gorlin syndrome [MESH:C538012] (133)
 Fetal Growth Retardation [MESH:D005317] (986)
 Hemorrhage [MESH:D006470] (4451) 
 Shock, Hemorrhagic [MESH:D012771] (2042)
 Hematoma [MESH:D006406] (281) 
 Hematoma, Epidural, Spinal [MESH:D046748] (167)
 Hematoma, Subdural [MESH:D006408] (215)
 Intracranial Hemorrhages [MESH:D020300] (3241) 
 Hematoma, Subdural [MESH:D006408] (212)
 Cerebral Hemorrhage [MESH:D002543] (2872) 
 Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)
 Hyperbilirubinemia [MESH:D006932] (1860) 
 Kernicterus [MESH:D007647] (256)
 Hyperbilirubinemia, Neonatal [MESH:D051556] (258) 
 Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)
 Jaundice [MESH:D007565] (316) 
 Jaundice, Obstructive [MESH:D041781] (176)
 Inflammation [MESH:D007249] (5241) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Systemic Inflammatory Response Syndrome [MESH:D018746] (3563) 
 Sepsis [MESH:D018805] (3562) 
 Shock, Septic [MESH:D012772] (1830)
 Bacteremia [MESH:D016470] (1369) 
 Endotoxemia [MESH:D019446] (1289)
 Ischemia [MESH:D007511] (3049) 
 No-Reflow Phenomenon [MESH:D054318] (277)
 Metaplasia [MESH:D008679] (1469) 
 Neovascularization, Pathologic [MESH:D009389] (829)
 Muscle Weakness [MESH:D018908] (478) 
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 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)
 Sclerosis [MESH:D012598] (224) 
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Shock [MESH:D012769] (2550) 
 Multiple Organ Failure [MESH:D009102] (1836)
 Shock, Cardiogenic [MESH:D012770] (269)
 Shock, Hemorrhagic [MESH:D012771] (2042)
 Systemic Inflammatory Response Syndrome [MESH:D018746] (1832) 
 Shock, Septic [MESH:D012772] (1830)
 Signs and Symptoms [MESH:D012816] (10659) 
 Chills [MESH:D023341] (644)
 Edema [MESH:D004487] (3726)
 Flushing [MESH:D005483] (506)
 Reticulocytosis [MESH:D045262] (514)
 Body Temperature Changes [MESH:D001832] (3130) 
 Fever [MESH:D005334] (2856)
 Hypothermia [MESH:D007035] (2075)
 Body Weight [MESH:D001835] (4972) 
 Body Weight Changes [MESH:D001836] (3206) 
 Weight Gain [MESH:D015430] (2595)
 Weight Loss [MESH:D015431] (2512) 
 Emaciation [MESH:D004614] (2285) 
 Cachexia [MESH:D002100] (2283)
 Overweight [MESH:D050177] (4455) 
 Obesity [MESH:D009765] (4454) 
 MORM syndrome [MESH:C536984] (15)
 Failure to Thrive [MESH:D005183] (415) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Neurologic Manifestations [MESH:D009461] (8702) 
 Gait Disorders, Neurologic [MESH:D020233] (491)
 Meningism [MESH:D008580] (43)
 Paresis [MESH:D010291] (419)
 Seizures [MESH:D012640] (4502)
 Dyskinesias [MESH:D020820] (3285) 
 Ataxia [MESH:D001259] (984)
 Catalepsy [MESH:D002375] (1429)
 Hyperkinesis [MESH:D006948] (1799)
 Neurobehavioral Manifestations [MESH:D019954] (4706) 
 Lethargy [MESH:D053609] (1035)
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Language Disorders [MESH:D007806] (653) 
 Speech Disorders [MESH:D013064] (482) 
 Aphasia [MESH:D001037] (219)
 Articulation Disorders [MESH:D001184] (164) 
 Dysarthria [MESH:D004401] (163)
 Confusion [MESH:D003221] (284) 
 Delirium [MESH:D003693] (173)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Intellectual Disability [MESH:D008607] (1476) 
 MORM syndrome [MESH:C536984] (15)
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Perceptual Disorders [MESH:D010468] (343) 
 Hallucinations [MESH:D006212] (251)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Fasciculation [MESH:D005207] (204)
 Muscle Cramp [MESH:D009120] (135)
 Muscular Atrophy [MESH:D009133] (1234)
 Muscle Weakness [MESH:D018908] (478) 
 Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of [MESH:C567006] (27)
 Pain [MESH:D010146] (3869) 
 Headache [MESH:D006261] (1417)
 Neuralgia [MESH:D009437] (2074)
 Back Pain [MESH:D001416] (285) 
 Low Back Pain [MESH:D017116] (244)
 Paralysis [MESH:D010243] (2298) 
 Gastroparesis [MESH:D018589] (732)
 Ophthalmoplegia [MESH:D009886] (1468) 
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)
 Sensation Disorders [MESH:D012678] (5009) 
 Hearing Disorders [MESH:D006311] (2101) 
 Hearing Loss [MESH:D034381] (2066)
 Somatosensory Disorders [MESH:D020886] (4000) 
 Hyperalgesia [MESH:D006930] (3929)
 Paresthesia [MESH:D010292] (416)
 Vision Disorders [MESH:D014786] (444) 
 Photophobia [MESH:D020795] (36)
 Sleep Disorders [MESH:D012893] (1301) 
 Sleep Deprivation [MESH:D012892] (233)
 Pain [MESH:D010146] (4511) 
 Arthralgia [MESH:D018771] (191)
 Headache [MESH:D006261] (1417)
 Neuralgia [MESH:D009437] (2074)
 Back Pain [MESH:D001416] (285) 
 Low Back Pain [MESH:D017116] (244)
 Chest Pain [MESH:D002637] (2642) 
 Angina Pectoris [MESH:D000787] (2568) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Angina, Stable [MESH:D060050] (1702)
 Signs and Symptoms, Digestive [MESH:D012817] (3095) 
 Diarrhea [MESH:D003967] (858)
 Nausea [MESH:D009325] (2300)
 Vomiting [MESH:D014839] (1354)
 Signs and Symptoms, Respiratory [MESH:D012818] (2724) 
 Anoxia [MESH:D000860] (1698)
 Dyspnea [MESH:D004417] (248)
 Hyperoxia [MESH:D018496] (694)
 Hyperventilation [MESH:D006985] (652) 
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Hypoventilation [MESH:D007040] (359) 
 Congenital central hypoventilation syndrome [MESH:C536209] (341)
 Skin Manifestations [MESH:D012877] (1250) 
 Pruritus [MESH:D011537] (648)
 Jaundice [MESH:D007565] (316) 
 Jaundice, Obstructive [MESH:D041781] (176)
 Urological Manifestations [MESH:D020924] (3532) 
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
C24. Occupational Diseases 
C24. Occupational Diseases
 Z. Exceptions (1530) 
 Not Fully Specified [NFS] (1530)
 Occupational Diseases [MESH:D009784] (3402) 
 Dermatitis, Occupational [MESH:D009783] (311)
 Pneumoconiosis [MESH:D011009] (2670) 
 Asbestosis [MESH:D001195] (935)
 Berylliosis [MESH:D001607] (2005)
 Silicosis [MESH:D012829] (1273)
C25. Chemically-Induced Disorders 
C25. Chemically-Induced Disorders
 Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839) 
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Drug Hypersensitivity [MESH:D004342] (4001) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 Drug Eruptions [MESH:D003875] (2697) 
 Serum Sickness [MESH:D012713] (484)
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 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)
 Substance-Related Disorders [MESH:D019966] (6308) 
 Amphetamine-Related Disorders [MESH:D019969] (2858)
 Cocaine-Related Disorders [MESH:D019970] (3054)
 Marijuana Abuse [MESH:D002189] (1132)
 Psychoses, Substance-Induced [MESH:D011605] (2052)
 Substance Withdrawal Syndrome [MESH:D013375] (2956)
 Alcohol-Related Disorders [MESH:D019973] (3869) 
 Alcohol-Induced Disorders [MESH:D020751] (3350) 
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 Fatty Liver, Alcoholic [MESH:D005235] (657)
 Hepatitis, Alcoholic [MESH:D006519] (1613)
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
C26. Wounds and Injuries 
C26. Wounds and Injuries
 Z. Exceptions (2454) 
 Not Fully Specified [NFS] (2454)
 Wounds and Injuries [MESH:D014947] (5171) 
 Burns [MESH:D002056] (2565)
 Vascular System Injuries [MESH:D057772] (2086)
 Craniocerebral Trauma [MESH:D006259] (3523) 
 Brain Injuries [MESH:D001930] (3431)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (217) 
 Hematoma, Subdural [MESH:D006408] (212)
 Fractures, Bone [MESH:D050723] (597) 
 Hip Fractures [MESH:D006620] (81)
 Femoral Fractures [MESH:D005264] (137) 
 Hip Fractures [MESH:D006620] (82)
 Hip Injuries [MESH:D025981] (83) 
 Hip Fractures [MESH:D006620] (81)
 Leg Injuries [MESH:D007869] (152) 
 Femoral Fractures [MESH:D005264] (137) 
 Hip Fractures [MESH:D006620] (82)
 Radiation Injuries [MESH:D011832] (2718) 
 Radiation Injuries, Experimental [MESH:D011833] (2662)
 Spinal Cord Injuries [MESH:D013119] (2688) 
 Spinal Cord Compression [MESH:D013117] (1800)
 Thoracic Injuries [MESH:D013898] (1831) 
 Lung Injury [MESH:D055370] (1814)
 Trauma, Nervous System [MESH:D020196] (3535) 
 Craniocerebral Trauma [MESH:D006259] (3507) 
 Brain Injuries [MESH:D001930] (3431)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (221) 
 Hematoma, Subdural [MESH:D006408] (212)
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) 
 Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (8627) 
 Indenes [MESH:D007192] (445) 
 Sulindac [MESH:D013467] (12)
D04. Polycyclic Compounds 
D04. Polycyclic Compounds
 Polycyclic Compounds [MESH:D011083] (22048) 
 Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (9200) 
 Indenes [MESH:D007192] (445) 
 Sulindac [MESH:D013467] (12)
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) 
 Body Constitution [MESH:D001824] (450) 
 Body Weights and Measures [MESH:D001837] (448) 
 Body Size [MESH:D049628] (439) 
 Body Weight [MESH:D001835] (433) 
 Overweight [MESH:D050177] (428) 
 Obesity [MESH:D009765] (427) 
 MORM syndrome [MESH:C536984] (15)
 Facies [MESH:D019066] (704) 
 Cardiofaciocutaneous syndrome [MESH:C535579] (407)
 Pitt-Hopkins syndrome [MESH:C537403] (113)
F. Psychiatry and Psychology 
F. Psychiatry and Psychology
 Behavior and Behavior Mechanisms [MESH:D001520] (1594) 
 Neurobehavioral Manifestations [MESH:D019954] (1206) 
 Intellectual Disability [MESH:D008607] (1109) 
 MORM syndrome [MESH:C536984] (15)
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Mental Disorders [MESH:D001523] (2063) 
 Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245) 
 Intellectual Disability [MESH:D008607] (1109) 
 MORM syndrome [MESH:C536984] (15)
 Pitt-Hopkins syndrome [MESH:C537403] (113)
 Mood Disorders [MESH:D019964] (257) 
 Affective Disorders, Psychotic [MESH:D000341] (248) 
 Bipolar Disorder [MESH:D001714] (247) 
 Major Affective Disorder 1 [MESH:C565111] (237)
 Major Affective Disorder 7 [MESH:C567529] (136)
G. Phenomena and Processes 
G. Phenomena and Processes
 Genetic Phenomena [MESH:D055614] (1922) 
 Genetic Processes [MESH:D039361] (1336) 
 Mutagenesis [MESH:D016296] (1150) 
 Sequence Deletion [MESH:D017384] (1120) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Genetic Structures [MESH:D040342] (1612) 
 Chromosomes [MESH:D002875] (1304) 
 Chromosomes, Mammalian [MESH:D033481] (1282) 
 Chromosomes, Human [MESH:D002877] (1280) 
 Chromosomes, Human, 16-18 [MESH:D002902] (799) 
 Chromosomes, Human, Pair 17 [MESH:D002886] (779) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Genetic Variation [MESH:D014644] (1337) 
 Mutation [MESH:D009154] (1327) 
 Allelic Imbalance [MESH:D022981] (1120) 
 Loss of Heterozygosity [MESH:D019656] (1119) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Chromosome Aberrations [MESH:D002869] (1297) 
 Aneuploidy [MESH:D000782] (1220) 
 Monosomy [MESH:D009006] (1121) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Sequence Deletion [MESH:D017384] (1120) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Ploidies [MESH:D011003] (1227) 
 Aneuploidy [MESH:D000782] (1220) 
 Monosomy [MESH:D009006] (1121) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Physiological Phenomena [MESH:D010829] (788) 
 Body Constitution [MESH:D001824] (453) 
 Body Weights and Measures [MESH:D001837] (444) 
 Body Size [MESH:D049628] (438) 
 Body Weight [MESH:D001835] (433) 
 Overweight [MESH:D050177] (428) 
 Obesity [MESH:D009765] (427) 
 MORM syndrome [MESH:C536984] (15)