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 cobaltiprotoporphyrin
C007095
 
  
  
  

MeSH Unique Identifier: C007095
Chemical – Gene Interaction

Note 1: Cobaltiprotoporphyrin inhibits the reaction [AGT protein results in increased phosphorylation of MAPK1 protein]

Note 2: Cobaltiprotoporphyrin inhibits the reaction [AGT protein results in increased phosphorylation of MAPK3 protein]

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C04. Neoplasms: Neoplasms [MESH:D009369] > Neoplastic Syndromes, Hereditary [MESH:D009386] > Meningioma, familial [MESH:C537443]
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1. Human Genes 
1. Human Genes
 Ankyrin repeat domain containing [HGNC:ANKRD] (566) 
 nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [HGNC:NFKBIA] (290)
 Basic leucine zipper proteins [HGNC:bZIP] (670) 
 FBJ murine osteosarcoma viral oncogene homolog [HGNC:FOS] (277)
 nuclear factor, erythroid 2-like 2 [HGNC:NFE2L2] (213)
 CD molecules [HGNC:CD] (1459) 
 intercellular adhesion molecule 1 [HGNC:ICAM1] (286)
 tumor necrosis factor receptor superfamily, member 01A [HGNC:TNFRSF1A] (72)
 vascular cell adhesion molecule 1 [HGNC:VCAM1] (172)
 Cytochrome P450s [HGNC:CYP] (1673) 
 cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566)
 Endogenous Ligands [HGNC:ENDOLIG] (1191) 
 interleukin 08 [HGNC:IL8] (649)
 High mobility group [HGNC:HMG] (101) 
 High mobility group, Canonical [HGNC:HMG] (98) 
 high mobility group box 1 [HGNC:HMGB1] (48)
 Immunoglobulin superfamily domain containing [HGNC:IGSF] (761) 
 C2-set domain containing [HGNC:C2SET] (225) 
 vascular cell adhesion molecule 1 [HGNC:VCAM1] (172)
 I-set domain containing [HGNC:ISET] (447) 
 vascular cell adhesion molecule 1 [HGNC:VCAM1] (172)
 Immunoglobulin-like domain containing [HGNC:IGD] (645) 
 intercellular adhesion molecule 1 [HGNC:ICAM1] (286)
 vascular cell adhesion molecule 1 [HGNC:VCAM1] (172)
 Interferons and interferon receptors [HGNC:IFN] (684) 
 interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)
 Interleukins and interleukin receptors [HGNC:IL] (1294) 
 interleukin 01, beta [HGNC:IL1B] (497)
 interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)
 interleukin 08 [HGNC:IL8] (649)
 interleukin 10 [HGNC:IL10] (187)
 interleukin 18 (interferon-gamma-inducing factor) [HGNC:IL18] (73)
 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)
 Protein tyrosine phosphatases, including dual specificity phosphatases [HGNC:PTP] (254) 
 Protein tyrosine phosphatases, Class I Cys-based [HGNC:PTPN] (252) 
 Class I Cys-based PTPs : PTENs [HGNC:DUSPQ] (91) 
 phosphatase and tensin homolog [HGNC:PTEN] (91)
 SH2 domain containing [HGNC:SH2D] (431) 
 v-src avian sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog [HGNC:SRC] (88)
 Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898) 
 tumor necrosis factor [HGNC:TNF] (795)
 Tumor necrosis factor receptor superfamily [HGNC:TNFRSF] (295) 
 tumor necrosis factor receptor superfamily, member 01A [HGNC:TNFRSF1A] (72)
 tumor necrosis factor receptor superfamily, member 11b [HGNC:TNFRSF11B] (63)
 ZINC FINGERS [HGNC:ZNF] (383) 
 Zinc fingers, C2H2-type [HGNC:ZNF] (349) 
 early growth response 1 [HGNC:EGR1] (140)
2. Interaction: Human Genes and Chemicals 
2. Interaction: Human Genes and Chemicals
 Affects (3990) 
 binding (2423)
 cotreatment (1499)
 expression (494)
 reaction (624)
 response to substance (623)
 Decreases (5154) 
 abundance (224)
 activity (2549)
 chemical synthesis (76)
 degradation (120)
 expression (2187)
 phosphorylation (590)
 reaction (3393)
 response to substance (713)
 secretion (346)
 Increases (5571) 
 abundance (630)
 activity (2865)
 cleavage (666)
 degradation (347)
 expression (3238)
 localization (244)
 phosphorylation (1060)
 reaction (1574)
 response to substance (641)
 secretion (901)
A. Anatomy 
A. Anatomy
 Body Regions [MESH:D001829] (867) 
 Head [MESH:D006257] (523) 
 Face [MESH:D005145] (387) 
 Kniest dysplasia [MESH:C537207] (89)
 Musculoskeletal System [MESH:D009141] (1255) 
 Skeleton [MESH:D012863] (1177) 
 Bone and Bones [MESH:D001842] (1112) 
 Spine [MESH:D013131] (258) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Digestive System [MESH:D004064] (421) 
 Gastrointestinal Tract [MESH:D041981] (364) 
 Intestines [MESH:D007422] (271) 
 Intestine, Large [MESH:D007420] (247) 
 Anal Canal [MESH:D001003] (217) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Lower Gastrointestinal Tract [MESH:D041741] (254) 
 Intestine, Large [MESH:D007420] (247) 
 Anal Canal [MESH:D001003] (217) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Upper Gastrointestinal Tract [MESH:D041742] (236) 
 Esophagus [MESH:D004947] (200) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Respiratory System [MESH:D012137] (321) 
 Trachea [MESH:D014132] (190) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Urogenital System [MESH:D014566] (986) 
 Urinary Tract [MESH:D014551] (721) 
 Kidney [MESH:D007668] (707) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 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)
 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) 
 Gram-Negative Bacterial Infections [MESH:D016905] (3085) 
 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) 
 Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)
 Tuberculosis [MESH:D014376] (992) 
 Tuberculosis, Bovine [MESH:D014380] (380)
 Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711) 
 Chlamydia Infections [MESH:D002690] (1693)
 Infection [MESH:D007239] (4109) 
 Arthritis, Infectious [MESH:D001170] (1702)
 Urinary Tract Infections [MESH:D014552] (984)
 Intraabdominal Infections [MESH:D059413] (958) 
 Appendicitis [MESH:D001064] (774)
 Peritonitis [MESH:D010538] (800)
 Sepsis [MESH:D018805] (3556) 
 Shock, Septic [MESH:D012772] (1830)
 Bacteremia [MESH:D016470] (1369) 
 Endotoxemia [MESH:D019446] (1289)
 Sexually Transmitted Diseases [MESH:D012749] (1712) 
 Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711) 
 Chlamydia Infections [MESH:D002690] (1693)
 Skin Diseases, Infectious [MESH:D012874] (415) 
 Dermatomycoses [MESH:D003881] (267) 
 Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)
 Toxemia [MESH:D014115] (1290) 
 Endotoxemia [MESH:D019446] (1289)
 Mycoses [MESH:D009181] (385) 
 Candidiasis [MESH:D002177] (307) 
 Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)
 Dermatomycoses [MESH:D003881] (267) 
 Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)
C02. Virus Diseases 
C02. Virus Diseases
 Virus Diseases [MESH:D014777] (4544) 
 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) 
 Cytomegalovirus Infections [MESH:D003586] (222)
 Sarcoma, Kaposi [MESH:D012514] (1578)
 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)
 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 Wasting Syndrome [MESH:D019247] (1956)
 Sexually Transmitted Diseases [MESH:D012749] (3305) 
 Sexually Transmitted Diseases, Viral [MESH:D015229] (3304) 
 HIV Infections [MESH:D015658] (3296) 
 Acquired Immunodeficiency Syndrome [MESH:D000163] (743)
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Slow Virus Diseases [MESH:D012897] (782) 
 Acquired Immunodeficiency Syndrome [MESH:D000163] (743)
 Tumor Virus Infections [MESH:D014412] (1069) 
 Papillomavirus Infections [MESH:D030361] (537)
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)
 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) 
 Hamartoma [MESH:D006222] (1484) 
 Tuberous Sclerosis [MESH:D014402] (635)
 Hamartoma Syndrome, Multiple [MESH:D006223] (262) 
 Proteus Syndrome [MESH:D016715] (152)
 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, Myeloid, Acute [MESH:D015470] (2176) 
 Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)
 Lymphoma [MESH:D008223] (3686) 
 Hodgkin Disease [MESH:D006689] (1082)
 Lymphoma, Non-Hodgkin [MESH:D008228] (3337) 
 Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Lymphoma, T-Cell [MESH:D016399] (1405) 
 Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)
 Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742) 
 Neoplasms, Adipose Tissue [MESH:D018205] (677) 
 Lipoma [MESH:D008067] (159)
 Neoplasms, Connective Tissue [MESH:D009372] (3626) 
 Chondrosarcoma [MESH:D002813] (1217)
 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, Aggressive [MESH:D018222] (1562)
 Neoplasms, Muscle Tissue [MESH:D009379] (1965) 
 Leiomyosarcoma [MESH:D007890] (977)
 Myosarcoma [MESH:D009217] (790) 
 Rhabdomyosarcoma [MESH:D012208] (789)
 Sarcoma [MESH:D012509] (4246) 
 Chondrosarcoma [MESH:D002813] (1217)
 Hemangiosarcoma [MESH:D006394] (1836)
 Leiomyosarcoma [MESH:D007890] (977)
 Osteosarcoma [MESH:D012516] (2175)
 Sarcoma, Kaposi [MESH:D012514] (1578)
 Myosarcoma [MESH:D009217] (790) 
 Rhabdomyosarcoma [MESH:D012208] (789)
 Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126) 
 Neuroectodermal Tumors [MESH:D017599] (5066) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Gliosarcoma [MESH:D018316] (880)
 Medulloblastoma [MESH:D008527] (1282)
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Medulloblastoma [MESH:D008527] (1282)
 Neuroendocrine Tumors [MESH:D018358] (3633) 
 Melanoma [MESH:D008545] (3508)
 Neoplasms, Glandular and Epithelial [MESH:D009375] (7760) 
 Adenoma [MESH:D000236] (4051) 
 Mesothelioma [MESH:D008654] (2567)
 Adenomatous Polyps [MESH:D018256] (1571) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Carcinoma [MESH:D002277] (7263) 
 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, Renal Cell [MESH:D002292] (2975)
 Cholangiocarcinoma [MESH:D018281] (2398)
 Adenocarcinoma, Follicular [MESH:D018263] (677) 
 Thyroid cancer, follicular [MESH:C572845] (674)
 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 in Situ [MESH:D002278] (2111) 
 Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)
 Carcinoma, Squamous Cell [MESH:D002294] (4294) 
 Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Neoplasms, Basal Cell [MESH:D018295] (1707) 
 Carcinoma, Basal Cell [MESH:D002280] (1628)
 Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831) 
 Carcinoma, Ductal [MESH:D044584] (1786) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Neoplasms, Mesothelial [MESH:D018301] (2569) 
 Mesothelioma [MESH:D008654] (2567)
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Gliosarcoma [MESH:D018316] (880)
 Medulloblastoma [MESH:D008527] (1282)
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Medulloblastoma [MESH:D008527] (1282)
 Neoplasms, Squamous Cell [MESH:D018307] (4457) 
 Papilloma [MESH:D010212] (2243)
 Carcinoma, Squamous Cell [MESH:D002294] (4294) 
 Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Neoplasms, Nerve Tissue [MESH:D009380] (5201) 
 Meningioma [MESH:D008579] (978) 
 Meningioma, familial [MESH:C537443] (195)
 Neuroectodermal Tumors [MESH:D017599] (5059) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Gliosarcoma [MESH:D018316] (880)
 Medulloblastoma [MESH:D008527] (1282)
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Medulloblastoma [MESH:D008527] (1282)
 Neuroendocrine Tumors [MESH:D018358] (3625) 
 Melanoma [MESH:D008545] (3508)
 Neoplasms, Plasma Cell [MESH:D054219] (2772) 
 Multiple Myeloma [MESH:D009101] (2767)
 Neoplasms, Vascular Tissue [MESH:D009383] (2959) 
 Hemangioma [MESH:D006391] (690)
 Hemangiosarcoma [MESH:D006394] (1836)
 Sarcoma, Kaposi [MESH:D012514] (1578)
 Meningioma [MESH:D008579] (978) 
 Meningioma, familial [MESH:C537443] (195)
 Nevi and Melanomas [MESH:D018326] (3572) 
 Melanoma [MESH:D008545] (3508)
 Neoplasms by Site [MESH:D009371] (9169) 
 Bone Neoplasms [MESH:D001859] (1334)
 Skin Neoplasms [MESH:D012878] (2992)
 Soft Tissue Neoplasms [MESH:D012983] (2003)
 Breast Neoplasms [MESH:D001943] (6077) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Digestive System Neoplasms [MESH:D004067] (7487) 
 Gastrointestinal Neoplasms [MESH:D005770] (6452) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Intestinal Neoplasms [MESH:D007414] (5358) 
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Liver Neoplasms [MESH:D008113] (6048) 
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Ovarian Neoplasms [MESH:D010051] (3275)
 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)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Thyroid Neoplasms [MESH:D013964] (2040) 
 Thyroid cancer, anaplastic [MESH:C536910] (489)
 Head and Neck Neoplasms [MESH:D006258] (4612) 
 Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Mouth Neoplasms [MESH:D009062] (2263) 
 Leukoplakia, Oral [MESH:D007972] (921)
 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)
 Mammary Neoplasms, Animal [MESH:D015674] (3404) 
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 Nervous System Neoplasms [MESH:D009423] (3130) 
 Central Nervous System Neoplasms [MESH:D016543] (3055) 
 Brain Neoplasms [MESH:D001932] (2764) 
 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) 
 Meningioma, familial [MESH:C537443] (195)
 Thoracic Neoplasms [MESH:D013899] (6032) 
 Respiratory Tract Neoplasms [MESH:D012142] (6020) 
 Lung Neoplasms [MESH:D008175] (6015) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Bronchial Neoplasms [MESH:D001984] (3608) 
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Small Cell Lung Carcinoma [MESH:D055752] (1380)
 Urogenital Neoplasms [MESH:D014565] (7002) 
 Genital Neoplasms, Female [MESH:D005833] (2540) 
 Vaginal Neoplasms [MESH:D014625] (363)
 Uterine Neoplasms [MESH:D014594] (2431) 
 Endometrial Neoplasms [MESH:D016889] (1987)
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Neoplasms [MESH:D011471] (6135)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Neoplasms, Experimental [MESH:D009374] (5218) 
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 Neoplasms, Multiple Primary [MESH:D009378] (961) 
 Tuberous Sclerosis [MESH:D014402] (635)
 Hamartoma Syndrome, Multiple [MESH:D006223] (262) 
 Proteus Syndrome [MESH:D016715] (152)
 Neoplastic Processes [MESH:D009385] (5317) 
 Neoplasm Invasiveness [MESH:D009361] (3388)
 Neoplasm Recurrence, Local [MESH:D009364] (1949)
 Neoplasm, Residual [MESH:D018365] (478)
 Carcinogenesis [MESH:D063646] (3391) 
 Cell Transformation, Neoplastic [MESH:D002471] (3389)
 Neoplasm Metastasis [MESH:D009362] (4441) 
 Lymphatic Metastasis [MESH:D008207] (917)
 Neoplastic Syndromes, Hereditary [MESH:D009386] (2578) 
 Meningioma, familial [MESH:C537443] (195)
 Juvenile polyposis syndrome [MESH:C537702] (196)
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Hamartoma Syndrome, Multiple [MESH:D006223] (260)
 Li-Fraumeni Syndrome [MESH:D016864] (859)
 Tuberous Sclerosis [MESH:D014402] (635)
 Precancerous Conditions [MESH:D011230] (2858) 
 Leukoplakia [MESH:D007971] (922) 
 Leukoplakia, Oral [MESH:D007972] (921)
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) 
 Proteus Syndrome [MESH:D016715] (152)
 Dwarfism [MESH:D004392] (778) 
 Kniest dysplasia [MESH:C537207] (89)
 Achondroplasia [MESH:D000130] (196) 
 Achondrogenesis type 2 [MESH:C536017] (89)
 Thanatophoric Dysplasia [MESH:D013796] (147) 
 Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)
 Dysostoses [MESH:D004413] (1019) 
 Synostosis [MESH:D013580] (817) 
 Craniosynostoses [MESH:D003398] (438)
 Osteochondrodysplasias [MESH:D010009] (2440) 
 Spondyloepiphyseal dysplasia, congenita [MESH:C535788] (89)
 Spondylometaphyseal dysplasia, Kozlowski type [MESH:C535797] (118)
 Kniest dysplasia [MESH:C537207] (89)
 Strudwick syndrome [MESH:C537501] (89)
 Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)
 Osteoarthritis with Mild Chondrodysplasia [MESH:C565740] (89)
 Spondyloepimetaphyseal Dysplasia, Missouri Type [MESH:C566574] (142)
 Fibrous Dysplasia of Bone [MESH:D005357] (737)
 Osteogenesis Imperfecta [MESH:D010013] (481)
 Achondroplasia [MESH:D000130] (196) 
 Achondrogenesis type 2 [MESH:C536017] (89)
 Thanatophoric Dysplasia [MESH:D013796] (147) 
 Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)
 Bone Diseases, Endocrine [MESH:D001849] (747) 
 Acromegaly [MESH:D000172] (466)
 Bone Diseases, Metabolic [MESH:D001851] (3492) 
 Osteoporosis [MESH:D010024] (3037) 
 Osteoporosis, Postmenopausal [MESH:D015663] (2351)
 Bone Resorption [MESH:D001862] (2352) 
 Osteolysis [MESH:D010014] (1787)
 Osteonecrosis [MESH:D010020] (539) 
 Femur Head Necrosis [MESH:D005271] (268) 
 Legg-Calve-Perthes Disease [MESH:D007873] (90)
 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) 
 Kniest dysplasia [MESH:C537207] (89)
 Joint Diseases [MESH:D007592] (4657) 
 Arthritis [MESH:D001168] (4416) 
 Stickler syndrome, type 1 [MESH:C537492] (89)
 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) 
 Osteoarthritis with Mild Chondrodysplasia [MESH:C565740] (89)
 Spondylarthritis [MESH:D025241] (1912) 
 Spondylarthropathies [MESH:D025242] (1909) 
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Muscular Diseases [MESH:D009135] (4071) 
 Compartment Syndromes [MESH:D003161] (80)
 Mitochondrial Myopathies [MESH:D017240] (2176) 
 Mitochondrial Encephalomyopathies [MESH:D017237] (1121) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Myositis [MESH:D009220] (2071) 
 Dermatomyositis [MESH:D003882] (1826)
 Polymyositis [MESH:D017285] (2007) 
 Dermatomyositis [MESH:D003882] (1826)
 Musculoskeletal Abnormalities [MESH:D009139] (3796) 
 Craniofacial Abnormalities [MESH:D019465] (3098) 
 Craniosynostoses [MESH:D003398] (438)
 LEOPARD Syndrome [MESH:D044542] (299)
 Macrocephaly [MESH:D058627] (264) 
 Macrocephaly Autism Syndrome [MESH:C565342] (151)
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330) 
 Kniest dysplasia [MESH:C537207] (89)
 Microcephaly [MESH:D008831] (700) 
 Amish lethal microcephaly [MESH:C538247] (29)
 Plagiocephaly [MESH:D059041] (440) 
 Craniosynostoses [MESH:D003398] (438)
 Limb Deformities, Congenital [MESH:D017880] (1813) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Polydactyly [MESH:D017689] (318)
 Proteus Syndrome [MESH:D016715] (152)
 Thanatophoric Dysplasia [MESH:D013796] (147) 
 Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)
 Synostosis [MESH:D013580] (817) 
 Craniosynostoses [MESH:D003398] (438)
 Rheumatic Diseases [MESH:D012216] (4032) 
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Osteoarthritis [MESH:D010003] (1743) 
 Osteoarthritis with Mild Chondrodysplasia [MESH:C565740] (89)
C06. Digestive System Diseases 
C06. Digestive System Diseases
 Digestive System Diseases [MESH:D004066] (9461) 
 Biliary Tract Diseases [MESH:D001660] (3845) 
 Bile Duct Diseases [MESH:D001649] (3512) 
 Cholestasis [MESH:D002779] (3419) 
 Cholestasis, Intrahepatic [MESH:D002780] (1510) 
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 Digestive System Abnormalities [MESH:D004065] (2127) 
 Barrett Esophagus [MESH:D001471] (1930)
 Digestive System Neoplasms [MESH:D004067] (7493) 
 Gastrointestinal Neoplasms [MESH:D005770] (6460) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Intestinal Neoplasms [MESH:D007414] (5359) 
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Liver Neoplasms [MESH:D008113] (6048) 
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 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)
 Deglutition Disorders [MESH:D003680] (1538) 
 Esophageal Motility Disorders [MESH:D015154] (1489) 
 Gastroesophageal Reflux [MESH:D005764] (1465)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Esophagitis [MESH:D004941] (1120) 
 Esophagitis, Peptic [MESH:D004942] (709)
 Gastroenteritis [MESH:D005759] (4066) 
 Appendicitis [MESH:D001064] (774)
 Mucositis [MESH:D052016] (1238)
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Enterocolitis [MESH:D004760] (1536) 
 Enterocolitis, Necrotizing [MESH:D020345] (1367)
 Esophagitis [MESH:D004941] (1120) 
 Esophagitis, Peptic [MESH:D004942] (709)
 Gastritis [MESH:D005756] (967) 
 Gastritis, Atrophic [MESH:D005757] (947)
 Inflammatory Bowel Diseases [MESH:D015212] (3492) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Crohn Disease [MESH:D003424] (2585)
 Gastrointestinal Hemorrhage [MESH:D006471] (815) 
 Peptic Ulcer Hemorrhage [MESH:D010438] (553)
 Gastrointestinal Neoplasms [MESH:D005770] (6460) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Intestinal Neoplasms [MESH:D007414] (5359) 
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Intestinal Diseases [MESH:D007410] (6206) 
 Intestinal Perforation [MESH:D007416] (471)
 Cecal Diseases [MESH:D002429] (1330) 
 Appendicitis [MESH:D001064] (774)
 Colonic Diseases [MESH:D003108] (5564) 
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Colonic Diseases, Functional [MESH:D003109] (439) 
 Irritable Bowel Syndrome [MESH:D043183] (429)
 Colorectal Neoplasms [MESH:D015179] (5282) 
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 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) 
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Intestinal Polyposis [MESH:D044483] (1610) 
 Juvenile polyposis syndrome [MESH:C537702] (196)
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Rectal Diseases [MESH:D012002] (4596) 
 Colorectal Neoplasms [MESH:D015179] (4534)
 Peptic Ulcer [MESH:D010437] (3172) 
 Duodenal Ulcer [MESH:D004381] (1549)
 Esophagitis, Peptic [MESH:D004942] (709)
 Stomach Ulcer [MESH:D013276] (2915)
 Stomach Diseases [MESH:D013272] (5325) 
 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)
 Hepatic Veno-Occlusive Disease [MESH:D006504] (208)
 Hepatorenal Syndrome [MESH:D006530] (910)
 Hypertension, Portal [MESH:D006975] (869)
 Liver Diseases, Parasitic [MESH:D008109] (1009)
 Cholestasis, Intrahepatic [MESH:D002780] (1510) 
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 Fatty Liver [MESH:D005234] (3584) 
 Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)
 Hepatic Insufficiency [MESH:D048550] (2771) 
 Liver Failure [MESH:D017093] (2768) 
 Hepatic Encephalopathy [MESH:D006501] (1795)
 Liver Failure, Acute [MESH:D017114] (2404)
 Hepatitis [MESH:D006505] (3883) 
 Hepatitis, Alcoholic [MESH:D006519] (1613)
 Hepatitis, Chronic [MESH:D006521] (2071) 
 Hepatitis, Autoimmune [MESH:D019693] (1982)
 Hepatitis, 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) 
 Hepatitis, Alcoholic [MESH:D006519] (1613)
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Liver Neoplasms [MESH:D008113] (6048) 
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Pancreatic Diseases [MESH:D010182] (4453) 
 Cystic Fibrosis [MESH:D003550] (760)
 Pancreatitis [MESH:D010195] (1924)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Peritoneal Diseases [MESH:D010532] (1119) 
 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) 
 Kniest dysplasia [MESH:C537207] (89)
 Mouth Diseases [MESH:D009059] (4783) 
 Behcet Syndrome [MESH:D001528] (1784)
 Mucositis [MESH:D052016] (1238)
 Oral Submucous Fibrosis [MESH:D009914] (2432)
 Lip Diseases [MESH:D008047] (924) 
 Cleft Lip [MESH:D002971] (914)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Lip [MESH:D002971] (914)
 Cleft Palate [MESH:D002972] (1330) 
 Kniest dysplasia [MESH:C537207] (89)
 Mouth Neoplasms [MESH:D009062] (2263) 
 Leukoplakia, Oral [MESH:D007972] (921)
 Tongue Neoplasms [MESH:D014062] (1518)
 Periodontal Diseases [MESH:D010510] (1001) 
 Gingival Diseases [MESH:D005882] (217) 
 Gingival Overgrowth [MESH:D019214] (192) 
 Gingival Hyperplasia [MESH:D005885] (161)
 Stomatitis [MESH:D013280] (1235) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Tongue Diseases [MESH:D014060] (1544) 
 Tongue Neoplasms [MESH:D014062] (1518)
 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) 
 Kniest dysplasia [MESH:C537207] (89)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Lip [MESH:D002971] (914)
 Cleft Palate [MESH:D002972] (1330) 
 Kniest dysplasia [MESH:C537207] (89)
C08. Respiratory Tract Diseases 
C08. Respiratory Tract Diseases
 Z. Exceptions (1984) 
 Not Fully Specified [NFS] (1984)
 Respiratory Tract Diseases [MESH:D012140] (7881) 
 Granuloma, Respiratory Tract [MESH:D015769] (502)
 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) 
 Bronchitis, Chronic [MESH:D029481] (569)
 Bronchiolitis [MESH:D001988] (617) 
 Bronchiolitis Obliterans [MESH:D001989] (611)
 Lung Diseases [MESH:D008171] (7249) 
 Cystic Fibrosis [MESH:D003550] (760)
 Hypertension, Pulmonary [MESH:D006976] (2000)
 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) 
 Bronchitis, Chronic [MESH:D029481] (569)
 Bronchiolitis [MESH:D001988] (617) 
 Bronchiolitis Obliterans [MESH:D001989] (611)
 Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564) 
 Bronchitis, Chronic [MESH:D029481] (569)
 Pulmonary Emphysema [MESH:D011656] (1259)
 Lung Injury [MESH:D055370] (3688) 
 Acute Lung Injury [MESH:D055371] (1907)
 Pneumoconiosis [MESH:D011009] (2789) 
 Anthracosis [MESH:D055008] (1805)
 Asbestosis [MESH:D001195] (935)
 Berylliosis [MESH:D001607] (2005)
 Silicosis [MESH:D012829] (1273)
 Ventilator-Induced Lung Injury [MESH:D055397] (1023) 
 Bronchopulmonary Dysplasia [MESH:D001997] (1021)
 Lung Neoplasms [MESH:D008175] (6012) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Small Cell Lung Carcinoma [MESH:D055752] (1380)
 Pneumonia [MESH:D011014] (3482) 
 Pneumonia, Aspiration [MESH:D011015] (824)
 Respiratory Distress Syndrome, Newborn [MESH:D012127] (169) 
 Hyaline Membrane Disease [MESH:D006819] (93) 
 Kniest dysplasia [MESH:C537207] (89)
 Nose Diseases [MESH:D009668] (1504) 
 Rhinitis [MESH:D012220] (1134)
 Pleural Diseases [MESH:D010995] (2240) 
 Pleurisy [MESH:D010998] (2070)
 Respiration Disorders [MESH:D012120] (2218) 
 Respiratory Distress Syndrome, Adult [MESH:D012128] (864)
 Respiratory Distress Syndrome, Newborn [MESH:D012127] (169) 
 Hyaline Membrane Disease [MESH:D006819] (93) 
 Kniest dysplasia [MESH:C537207] (89)
 Respiratory Hypersensitivity [MESH:D012130] (4401) 
 Alveolitis, Extrinsic Allergic [MESH:D000542] (495)
 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)
 Rhinitis [MESH:D012220] (766)
 Bronchitis [MESH:D001991] (588) 
 Bronchitis, Chronic [MESH:D029481] (569)
 Legionellosis [MESH:D007876] (612) 
 Legionnaires' Disease [MESH:D007877] (611)
 Pneumonia [MESH:D011014] (3482) 
 Pneumonia, Aspiration [MESH:D011015] (824)
 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) 
 Ear Diseases [MESH:D004427] (2522) 
 Hearing Disorders [MESH:D006311] (2103) 
 Hearing Loss [MESH:D034381] (2068) 
 Hearing Loss, Conductive [MESH:D006314] (134) 
 Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)
 Hearing Loss, Sensorineural [MESH:D006319] (1227) 
 Stickler syndrome, type 1 [MESH:C537492] (89)
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Labyrinth Diseases [MESH:D007759] (846) 
 Vestibular Diseases [MESH:D015837] (819)
 Nose Diseases [MESH:D009668] (1504) 
 Rhinitis [MESH:D012220] (1134)
 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) 
 Sleep Disorders [MESH:D012893] (2050)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810) 
 Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)
 Central Nervous System Diseases [MESH:D002493] (9745) 
 Brain Diseases [MESH:D001927] (9294) 
 Brain Edema [MESH:D001929] (1165)
 Brain Injuries [MESH:D001930] (3429)
 Basal Ganglia Diseases [MESH:D001480] (4268) 
 Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)
 Parkinsonian Disorders [MESH:D020734] (4009) 
 Lewy Body Disease [MESH:D020961] (1143)
 Parkinson Disease [MESH:D010300] (3595)
 Brain Diseases, Metabolic [MESH:D001928] (3351) 
 Hepatic Encephalopathy [MESH:D006501] (1795)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Peroxisomal Disorders [MESH:D018901] (1472) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Brain Neoplasms [MESH:D001932] (2764) 
 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)
 Cerebrovascular Disorders [MESH:D002561] (5542) 
 Carotid Artery Diseases [MESH:D002340] (1993)
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Brain Ischemia [MESH:D002545] (4873) 
 Ischemic Attack, Transient [MESH:D002546] (1313)
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Cerebral Small Vessel Diseases [MESH:D059345] (1292) 
 MELAS Syndrome [MESH:D017241] (1061)
 Intracranial Arterial Diseases [MESH:D020765] (2463) 
 Intracranial Aneurysm [MESH:D002532] (158)
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873)
 Subarachnoid Hemorrhage [MESH:D013345] (1082)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Dementia [MESH:D003704] (4498) 
 Alzheimer Disease [MESH:D000544] (4275)
 Lewy Body Disease [MESH:D020961] (1143)
 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)
 Headache Disorders [MESH:D020773] (2337) 
 Headache Disorders, Primary [MESH:D051270] (2327) 
 Migraine Disorders [MESH:D008881] (2318)
 Hydrocephalus [MESH:D006849] (276) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Hypothalamic Diseases [MESH:D007027] (1833) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Pituitary Diseases [MESH:D010900] (1808) 
 Pituitary Neoplasms [MESH:D010911] (981)
 Hyperpituitarism [MESH:D006964] (1250) 
 Acromegaly [MESH:D000172] (466)
 Intracranial Hypertension [MESH:D019586] (368) 
 Hydrocephalus [MESH:D006849] (274) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Leukoencephalopathies [MESH:D056784] (1916) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822) 
 Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Central Nervous System Infections [MESH:D002494] (1823) 
 Central Nervous System Viral Diseases [MESH:D020805] (1416) 
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Meningitis [MESH:D008581] (1506) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Movement Disorders [MESH:D009069] (4823) 
 Dyskinesias [MESH:D020820] (1827) 
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 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) 
 Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)
 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)
 Malformations of Cortical Development [MESH:D054220] (1406) 
 Tuberous Sclerosis [MESH:D014402] (635)
 Macrocephaly [MESH:D058627] (264) 
 Macrocephaly Autism Syndrome [MESH:C565342] (151)
 Microcephaly [MESH:D008831] (700) 
 Amish lethal microcephaly [MESH:C538247] (29)
 Nervous System Neoplasms [MESH:D009423] (3073) 
 Central Nervous System Neoplasms [MESH:D016543] (3055) 
 Brain Neoplasms [MESH:D001932] (2764) 
 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) 
 Meningioma, familial [MESH:C537443] (195)
 Neurocutaneous Syndromes [MESH:D020752] (1230) 
 Tuberous Sclerosis [MESH:D014402] (635)
 Neurodegenerative Diseases [MESH:D019636] (6613) 
 Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)
 Lewy Body Disease [MESH:D020961] (1143)
 Parkinson Disease [MESH:D010300] (3595)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243) 
 Tuberous Sclerosis [MESH:D014402] (635)
 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)
 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)
 Neurologic Manifestations [MESH:D009461] (8964) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Reflex, Abnormal [MESH:D012021] (485)
 Seizures [MESH:D012640] (4514)
 Dyskinesias [MESH:D020820] (3365) 
 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) 
 Language Development Disorders [MESH:D007805] (351)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Intellectual Disability [MESH:D008607] (3054) 
 Down Syndrome [MESH:D004314] (1287)
 Mental Retardation, X-Linked [MESH:D038901] (1854) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Muscular Atrophy [MESH:D009133] (1234)
 Pain [MESH:D010146] (3875) 
 Headache [MESH:D006261] (1416)
 Pain, Intractable [MESH:D010148] (707)
 Back Pain [MESH:D001416] (287) 
 Low Back Pain [MESH:D017116] (244)
 Neuralgia [MESH:D009437] (2074) 
 Neuralgia, Postherpetic [MESH:D051474] (742)
 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) 
 Hearing Loss, Conductive [MESH:D006314] (134) 
 Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)
 Hearing Loss, Sensorineural [MESH:D006319] (1227) 
 Stickler syndrome, type 1 [MESH:C537492] (89)
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Somatosensory Disorders [MESH:D020886] (4000) 
 Hyperalgesia [MESH:D006930] (3929)
 Neuromuscular Diseases [MESH:D009468] (7336) 
 Motor Neuron Disease [MESH:D016472] (3670) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Muscular Diseases [MESH:D009135] (3538) 
 Mitochondrial Myopathies [MESH:D017240] (2176) 
 Mitochondrial Encephalomyopathies [MESH:D017237] (1121) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Myositis [MESH:D009220] (2069) 
 Dermatomyositis [MESH:D003882] (1826)
 Polymyositis [MESH:D017285] (2007) 
 Dermatomyositis [MESH:D003882] (1826)
 Peripheral Nervous System Diseases [MESH:D010523] (6151) 
 Diabetic Neuropathies [MESH:D003929] (2442)
 Neuralgia [MESH:D009437] (2078) 
 Neuralgia, Postherpetic [MESH:D051474] (742)
 Neurotoxicity Syndromes [MESH:D020258] (4570) 
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912) 
 Arsenic Poisoning [MESH:D020261] (2540)
 Manganese Poisoning [MESH:D020149] (2214)
 Trauma, Nervous System [MESH:D020196] (3997) 
 Spinal Cord Injuries [MESH:D013119] (1676)
 Craniocerebral Trauma [MESH:D006259] (3507) 
 Brain Injuries [MESH:D001930] (3431)
C11. Eye Diseases 
C11. Eye Diseases
 Eye Diseases [MESH:D005128] (6245) 
 Eyelid Diseases [MESH:D005141] (882)
 Corneal Diseases [MESH:D003316] (1445) 
 Corneal Neovascularization [MESH:D016510] (622)
 Eye Diseases, Hereditary [MESH:D015785] (1869) 
 Stickler Syndrome, Type I, Nonsyndromic Ocular [MESH:C563709] (89)
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Lens Diseases [MESH:D007905] (900) 
 Cataract [MESH:D002386] (860)
 Ocular Hypertension [MESH:D009798] (1630) 
 Glaucoma [MESH:D005901] (1458) 
 Glaucoma, Open-Angle [MESH:D005902] (1281)
 Ocular Motility Disorders [MESH:D015835] (1699) 
 Ophthalmoplegia [MESH:D009886] (1468) 
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)
 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)
 Refractive Errors [MESH:D012030] (457) 
 Anisometropia [MESH:D015858] (152)
 Myopia [MESH:D009216] (349) 
 Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)
 Retinal Diseases [MESH:D012164] (3747) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Retinal Vein Occlusion [MESH:D012170] (607)
 Retinopathy of Prematurity [MESH:D012178] (353)
 Retinal Degeneration [MESH:D012162] (2386) 
 Hyaloideoretinal degeneration of Wagner [MESH:C536075] (135)
 Macular Degeneration [MESH:D008268] (995) 
 Macular Edema [MESH:D008269] (557)
 Retinal Dystrophies [MESH:D058499] (1315) 
 Retinitis Pigmentosa [MESH:D012174] (1307) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Retinal Detachment [MESH:D012163] (1639) 
 Stickler syndrome, type 1 [MESH:C537492] (89)
 Uveal Diseases [MESH:D014603] (2428) 
 Choroid Diseases [MESH:D015862] (595) 
 Choroidal Neovascularization [MESH:D020256] (550)
 Uveitis [MESH:D014605] (2157) 
 Panuveitis [MESH:D015864] (1805) 
 Uveitis, Anterior [MESH:D014606] (1791) 
 Behcet Syndrome [MESH:D001528] (1784)
C12. Male Urogenital Diseases 
C12. Male Urogenital Diseases
 Male Urogenital Diseases [MESH:D052801] (8891) 
 Genital Diseases, Male [MESH:D005832] (6794) 
 Testicular Diseases [MESH:D013733] (451)
 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)
 Penile Diseases [MESH:D010409] (1805) 
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Diseases [MESH:D011469] (6204) 
 Prostatic Neoplasms [MESH:D011471] (6135)
 Prostatitis [MESH:D011472] (424)
 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)
 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) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Urologic Diseases [MESH:D014570] (7792) 
 Urinary Tract Infections [MESH:D014552] (984)
 Kidney Diseases [MESH:D007674] (7242) 
 Anuria [MESH:D001002] (833)
 Diabetic Nephropathies [MESH:D003928] (2301)
 Hepatorenal Syndrome [MESH:D006530] (910)
 Hydronephrosis [MESH:D006869] (956)
 Hyperoxaluria [MESH:D006959] (1498)
 Hypertension, Renal [MESH:D006977] (698) 
 Hypertension, Renovascular [MESH:D006978] (365)
 Kidney Diseases, Cystic [MESH:D052177] (1009) 
 Polycystic Kidney Diseases [MESH:D007690] (853) 
 Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758) 
 Glomerulonephritis, IGA [MESH:D005922] (897)
 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)
 Uremia [MESH:D014511] (2898) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435) 
 Atypical hemolytic uremic syndrome [MESH:C538266] (277)
 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)
 Polyuria [MESH:D011141] (279)
 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 Neoplasms [MESH:D010051] (3281)
 Infertility [MESH:D007246] (2211) 
 Infertility, Female [MESH:D007247] (2184)
 Sexually Transmitted Diseases [MESH:D012749] (1712) 
 Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711) 
 Chlamydia Infections [MESH:D002690] (1693)
 Uterine Diseases [MESH:D014591] (2479) 
 Endometrial Hyperplasia [MESH:D004714] (263)
 Uterine Cervical Diseases [MESH:D002577] (988) 
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Uterine Neoplasms [MESH:D014594] (2430) 
 Endometrial Neoplasms [MESH:D016889] (1984)
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Vaginal Diseases [MESH:D014623] (446) 
 Vaginal Neoplasms [MESH:D014625] (363)
 Vulvar Diseases [MESH:D014845] (873) 
 Vulvar Lichen Sclerosus [MESH:D007724] (825)
 Urogenital Abnormalities [MESH:D014564] (2043) 
 Allanson Pantzar McLeod syndrome [MESH:C537048] (503)
 Urogenital Neoplasms [MESH:D014565] (5792) 
 Genital Neoplasms, Female [MESH:D005833] (3810) 
 Ovarian Neoplasms [MESH:D010051] (3281)
 Vaginal Neoplasms [MESH:D014625] (363)
 Uterine Neoplasms [MESH:D014594] (2433) 
 Endometrial Neoplasms [MESH:D016889] (1989)
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Urologic Diseases [MESH:D014570] (7793) 
 Urinary Tract Infections [MESH:D014552] (984)
 Kidney Diseases [MESH:D007674] (7242) 
 Anuria [MESH:D001002] (833)
 Diabetic Nephropathies [MESH:D003928] (2301)
 Hepatorenal Syndrome [MESH:D006530] (910)
 Hydronephrosis [MESH:D006869] (956)
 Hyperoxaluria [MESH:D006959] (1498)
 Hypertension, Renal [MESH:D006977] (698) 
 Hypertension, Renovascular [MESH:D006978] (365)
 Kidney Diseases, Cystic [MESH:D052177] (1009) 
 Polycystic Kidney Diseases [MESH:D007690] (853) 
 Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758) 
 Glomerulonephritis, IGA [MESH:D005922] (897)
 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)
 Uremia [MESH:D014511] (2898) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435) 
 Atypical hemolytic uremic syndrome [MESH:C538266] (277)
 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)
 Polyuria [MESH:D011141] (279)
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
 Pregnancy Complications [MESH:D011248] (4768) 
 Abortion, Spontaneous [MESH:D000022] (2780)
 Diabetes, Gestational [MESH:D016640] (1157)
 Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)
 Prenatal Injuries [MESH:D049188] (1314)
 Fetal Diseases [MESH:D005315] (1206) 
 Fetal Growth Retardation [MESH:D005317] (986)
 Hypertension, Pregnancy-Induced [MESH:D046110] (1453) 
 Pre-Eclampsia [MESH:D011225] (1435)
 Obstetric Labor Complications [MESH:D007744] (1550) 
 Abruptio Placentae [MESH:D000037] (430)
 Obstetric Labor, Premature [MESH:D007752] (1316)
 Placenta Diseases [MESH:D010922] (1781) 
 Abruptio Placentae [MESH:D000037] (430)
C14. Cardiovascular Diseases 
C14. Cardiovascular Diseases
 Z. Exceptions (2667) 
 Not Fully Specified [NFS] (2667)
 Cardiovascular Diseases [MESH:D002318] (10123) 
 Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)
 Cardiovascular Abnormalities [MESH:D018376] (3153) 
 Heart Defects, Congenital [MESH:D006330] (2447) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 LEOPARD Syndrome [MESH:D044542] (299)
 Vascular Malformations [MESH:D054079] (1098) 
 Arteriovenous Malformations [MESH:D001165] (1058) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Central Nervous System Vascular Malformations [MESH:D020785] (1031) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Heart Diseases [MESH:D006331] (8614) 
 Heart Arrest [MESH:D006323] (1926)
 Heart Failure [MESH:D006333] (4058)
 Pericardial Effusion [MESH:D010490] (1015)
 Arrhythmias, Cardiac [MESH:D001145] (4679) 
 Atrial Fibrillation [MESH:D001281] (1053)
 Bradycardia [MESH:D001919] (1899)
 Long QT Syndrome [MESH:D008133] (693)
 Cardiac Complexes, Premature [MESH:D005117] (429) 
 Ventricular Premature Complexes [MESH:D018879] (418)
 Tachycardia [MESH:D013610] (3339) 
 Tachycardia, Ventricular [MESH:D017180] (1386)
 Cardiomegaly [MESH:D006332] (4081) 
 Cardiomyopathy, Dilated [MESH:D002311] (1576)
 Hypertrophy, Left Ventricular [MESH:D017379] (1430)
 Cardiomyopathies [MESH:D009202] (5331) 
 Cardiomyopathy, Alcoholic [MESH:D002310] (354)
 Cardiomyopathy, Dilated [MESH:D002311] (1576)
 Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)
 Diabetic Cardiomyopathies [MESH:D058065] (1995)
 Endomyocardial Fibrosis [MESH:D004719] (521)
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Myocarditis [MESH:D009205] (1708)
 Heart Defects, Congenital [MESH:D006330] (2443) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 LEOPARD Syndrome [MESH:D044542] (299)
 Heart Valve Diseases [MESH:D006349] (3333) 
 Aortic Valve Stenosis [MESH:D001024] (1742) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Aortic Stenosis, Subvalvular [MESH:D001020] (1455) 
 Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)
 Pulmonary Valve Stenosis [MESH:D011666] (360) 
 LEOPARD Syndrome [MESH:D044542] (299)
 Myocardial Ischemia [MESH:D017202] (5787) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Myocardial Stunning [MESH:D017682] (1816)
 Angina Pectoris [MESH:D000787] (2575) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Angina, Unstable [MESH:D000789] (782)
 Angina, Stable [MESH:D060050] (1702)
 Coronary Disease [MESH:D003327] (3439) 
 Coronary Artery Disease [MESH:D003324] (2685)
 Coronary Vasospasm [MESH:D003329] (533)
 Coronary Stenosis [MESH:D023921] (1806) 
 Coronary Restenosis [MESH:D023903] (1683)
 Myocardial Infarction [MESH:D009203] (4122) 
 Myocardial Stunning [MESH:D017682] (1816)
 Ventricular Dysfunction [MESH:D018754] (2348) 
 Ventricular Dysfunction, Left [MESH:D018487] (1631)
 Ventricular Outflow Obstruction [MESH:D014694] (976) 
 Aortic Valve Stenosis [MESH:D001024] (810) 
 Aortic Valve, Calcification of [MESH:C562942] (655)
 Vascular Diseases [MESH:D014652] (8691) 
 Arteritis [MESH:D001167] (1084)
 Compartment Syndromes [MESH:D003161] (80)
 Hepatic Veno-Occlusive Disease [MESH:D006504] (208)
 Hyperemia [MESH:D006940] (2372)
 Hypotension [MESH:D007022] (4045)
 Peripheral Vascular Diseases [MESH:D016491] (1412)
 Retinal Vein Occlusion [MESH:D012170] (607)
 Vascular System Injuries [MESH:D057772] (2086)
 Aneurysm [MESH:D000783] (1886) 
 Aneurysm, Dissecting [MESH:D000784] (699)
 Intracranial Aneurysm [MESH:D002532] (158)
 Aortic Aneurysm [MESH:D001014] (1721) 
 Aortic Aneurysm, Abdominal [MESH:D017544] (1519)
 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) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Cerebrovascular Disorders [MESH:D002561] (5541) 
 Carotid Artery Diseases [MESH:D002340] (1993)
 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)
 Cerebral Small Vessel Diseases [MESH:D059345] (1292) 
 MELAS Syndrome [MESH:D017241] (1061)
 Intracranial Arterial Diseases [MESH:D020765] (2468) 
 Intracranial Aneurysm [MESH:D002532] (158)
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873)
 Subarachnoid Hemorrhage [MESH:D013345] (1082)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Diabetic Angiopathies [MESH:D003925] (1984) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Embolism and Thrombosis [MESH:D016769] (3374) 
 Embolism [MESH:D004617] (1137) 
 Pulmonary Embolism [MESH:D011655] (1118)
 Thrombosis [MESH:D013927] (3101) 
 Venous Thrombosis [MESH:D020246] (1141) 
 Retinal Vein Occlusion [MESH:D012170] (607)
 Hemostatic Disorders [MESH:D020141] (2894) 
 Multiple Myeloma [MESH:D009101] (2765)
 Hypertension [MESH:D006973] (5655) 
 Hypertension, Essential [MESH:C562386] (1308)
 Hypertension, Malignant [MESH:D006974] (621)
 Hypertension, Pregnancy-Induced [MESH:D046110] (397)
 Hypertension, Renal [MESH:D006977] (698) 
 Hypertension, Renovascular [MESH:D006978] (365)
 Myocardial Ischemia [MESH:D017202] (5791) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Myocardial Stunning [MESH:D017682] (1816)
 Angina Pectoris [MESH:D000787] (2575) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Angina, Unstable [MESH:D000789] (782)
 Angina, Stable [MESH:D060050] (1702)
 Coronary Disease [MESH:D003327] (3439) 
 Coronary Artery Disease [MESH:D003324] (2685)
 Coronary Vasospasm [MESH:D003329] (533)
 Coronary Stenosis [MESH:D023921] (1806) 
 Coronary Restenosis [MESH:D023903] (1683)
 Myocardial Infarction [MESH:D009203] (4151) 
 Myocardial Stunning [MESH:D017682] (1816)
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 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) 
 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) 
 Anemia, Hemolytic, Congenital [MESH:D000745] (2001) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435) 
 Atypical hemolytic uremic syndrome [MESH:C538266] (277)
 Blood Coagulation Disorders [MESH:D001778] (1828) 
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Thrombocythemia, Essential [MESH:D013920] (707)
 Purpura [MESH:D011693] (475) 
 Purpura, Thrombocytopenic [MESH:D011696] (237) 
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Blood Platelet Disorders [MESH:D001791] (3174) 
 Thrombocytopenia [MESH:D013921] (2966) 
 Thrombotic Microangiopathies [MESH:D057049] (2598) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435) 
 Atypical hemolytic uremic syndrome [MESH:C538266] (277)
 Purpura, Thrombocytopenic [MESH:D011696] (237) 
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Thrombocytosis [MESH:D013922] (720) 
 Thrombocythemia, Essential [MESH:D013920] (707)
 Blood Protein Disorders [MESH:D001796] (3051) 
 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) 
 Thrombocytosis [MESH:D013922] (720) 
 Thrombocythemia, Essential [MESH:D013920] (707)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Hemorrhagic Disorders [MESH:D006474] (3359) 
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Thrombocythemia, Essential [MESH:D013920] (707)
 Hemostatic Disorders [MESH:D020141] (2932) 
 Multiple Myeloma [MESH:D009101] (2765)
 Leukocyte Disorders [MESH:D007960] (2662) 
 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) 
 Granulomatous Disease, Chronic [MESH:D006105] (404) 
 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142)
 Job Syndrome [MESH:D007589] (772) 
 Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)
 Thrombophilia [MESH:D019851] (592) 
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Lymphatic Diseases [MESH:D008206] (5167) 
 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) 
 Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities 
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
 Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152) 
 Congenital Abnormalities [MESH:D000013] (8109) 
 Abnormalities, Drug-Induced [MESH:D000014] (1024)
 Abnormalities, Multiple [MESH:D000015] (3192) 
 Down Syndrome [MESH:D004314] (1287)
 LEOPARD Syndrome [MESH:D044542] (299)
 Proteus Syndrome [MESH:D016715] (152)
 Ectodermal Dysplasia [MESH:D004476] (938) 
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Cardiovascular Abnormalities [MESH:D018376] (3294) 
 Heart Defects, Congenital [MESH:D006330] (2611) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 LEOPARD Syndrome [MESH:D044542] (299)
 Long QT Syndrome [MESH:D008133] (693)
 Vascular Malformations [MESH:D054079] (1108) 
 Arteriovenous Malformations [MESH:D001165] (1058) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Central Nervous System Vascular Malformations [MESH:D020785] (1018) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Chromosome Disorders [MESH:D025063] (2030) 
 Down Syndrome [MESH:D004314] (1287)
 Musculoskeletal Abnormalities [MESH:D009139] (3779) 
 Craniofacial Abnormalities [MESH:D019465] (3064) 
 Craniosynostoses [MESH:D003398] (438)
 LEOPARD Syndrome [MESH:D044542] (299)
 Macrocephaly [MESH:D058627] (264) 
 Macrocephaly Autism Syndrome [MESH:C565342] (151)
 Maxillofacial Abnormalities [MESH:D019767] (1448) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330) 
 Kniest dysplasia [MESH:C537207] (89)
 Microcephaly [MESH:D008831] (700) 
 Amish lethal microcephaly [MESH:C538247] (29)
 Plagiocephaly [MESH:D059041] (440) 
 Craniosynostoses [MESH:D003398] (438)
 Limb Deformities, Congenital [MESH:D017880] (1813) 
 VACTERL hydrocephaly [MESH:C536521] (151)
 Polydactyly [MESH:D017689] (318)
 Proteus Syndrome [MESH:D016715] (152)
 Thanatophoric Dysplasia [MESH:D013796] (147) 
 Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)
 Synostosis [MESH:D013580] (817) 
 Craniosynostoses [MESH:D003398] (438)
 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)
 Malformations of Cortical Development [MESH:D054220] (1406) 
 Tuberous Sclerosis [MESH:D014402] (635)
 Macrocephaly [MESH:D058627] (264) 
 Macrocephaly Autism Syndrome [MESH:C565342] (151)
 Microcephaly [MESH:D008831] (700) 
 Amish lethal microcephaly [MESH:C538247] (29)
 Skin Abnormalities [MESH:D012868] (1723) 
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330) 
 Kniest dysplasia [MESH:C537207] (89)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Lip [MESH:D002971] (914)
 Cleft Palate [MESH:D002972] (1330) 
 Kniest dysplasia [MESH:C537207] (89)
 Urogenital Abnormalities [MESH:D014564] (2064) 
 Allanson Pantzar McLeod syndrome [MESH:C537048] (503)
 Fetal Diseases [MESH:D005315] (1205) 
 Fetal Growth Retardation [MESH:D005317] (986)
 Genetic Diseases, Inborn [MESH:D030342] (9766) 
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Cystic Fibrosis [MESH:D003550] (760)
 Osteogenesis Imperfecta [MESH:D010013] (481)
 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)
 Chromosome Disorders [MESH:D025063] (2030) 
 Down Syndrome [MESH:D004314] (1287)
 Dwarfism [MESH:D004392] (783) 
 Kniest dysplasia [MESH:C537207] (89)
 Achondroplasia [MESH:D000130] (196) 
 Achondrogenesis type 2 [MESH:C536017] (89)
 Thanatophoric Dysplasia [MESH:D013796] (147) 
 Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)
 Eye Diseases, Hereditary [MESH:D015785] (1867) 
 Stickler Syndrome, Type I, Nonsyndromic Ocular [MESH:C563709] (89)
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Genetic Diseases, X-Linked [MESH:D040181] (3028) 
 Granulomatous Disease, Chronic [MESH:D006105] (404) 
 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142)
 Mental Retardation, X-Linked [MESH:D038901] (1867) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Hereditary Autoinflammatory Diseases [MESH:D056660] (272) 
 Periodic fever, familial, autosomal dominant [MESH:C536657] (177)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465) 
 Tuberous Sclerosis [MESH:D014402] (635)
 Mental Retardation, X-Linked [MESH:D038901] (1848) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 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) 
 Myeloperoxidase Deficiency [MESH:C562864] (335)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565) 
 Methylmalonic acidemia [MESH:C537358] (764)
 Hyperhomocysteinemia [MESH:D020138] (1724)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Peroxisomal Disorders [MESH:D018901] (1472) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)
 Hyperlipidemia, Familial Combined [MESH:D006950] (372)
 Lipidoses [MESH:D008064] (1655) 
 Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026) 
 Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)
 Metal Metabolism, Inborn Errors [MESH:D008664] (2017) 
 Hemochromatosis [MESH:D006432] (1694)
 Peroxisomal Disorders [MESH:D018901] (1788) 
 Acatalasia [MESH:D020642] (788)
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Neoplastic Syndromes, Hereditary [MESH:D009386] (2578) 
 Meningioma, familial [MESH:C537443] (195)
 Juvenile polyposis syndrome [MESH:C537702] (196)
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Hamartoma Syndrome, Multiple [MESH:D006223] (260)
 Li-Fraumeni Syndrome [MESH:D016864] (859)
 Tuberous Sclerosis [MESH:D014402] (635)
 Skin Diseases, Genetic [MESH:D012873] (3456) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Infant, Newborn, Diseases [MESH:D007232] (3064) 
 Asphyxia Neonatorum [MESH:D001238] (1648)
 Cystic Fibrosis [MESH:D003550] (760)
 Infant, Premature, Diseases [MESH:D007235] (1292) 
 Bronchopulmonary Dysplasia [MESH:D001997] (1021)
 Retinopathy of Prematurity [MESH:D012178] (353)
 Respiratory Distress Syndrome, Newborn [MESH:D012127] (169) 
 Hyaline Membrane Disease [MESH:D006819] (93) 
 Kniest dysplasia [MESH:C537207] (89)
 Thanatophoric Dysplasia [MESH:D013796] (147) 
 Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)
C17. Skin and Connective Tissue Diseases 
C17. Skin and Connective Tissue Diseases
 Connective Tissue Diseases [MESH:D003240] (4490) 
 Stickler syndrome, type 1 [MESH:C537492] (89)
 Dermatomyositis [MESH:D003882] (1826)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317)
 Scleroderma, Localized [MESH:D012594] (1597)
 Collagen Diseases [MESH:D003095] (1267) 
 Kniest dysplasia [MESH:C537207] (89)
 Osteogenesis Imperfecta [MESH:D010013] (481)
 Rheumatic Diseases [MESH:D012216] (3619) 
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Skin Diseases [MESH:D012871] (8774) 
 Dermatomyositis [MESH:D003882] (1826)
 Keratosis [MESH:D007642] (1941)
 Lipomatosis [MESH:D008068] (182)
 Scleroderma, Localized [MESH:D012594] (1597)
 Skin Neoplasms [MESH:D012878] (2991)
 Breast Diseases [MESH:D001941] (6148) 
 Breast Neoplasms [MESH:D001943] (6077) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Dermatitis [MESH:D003872] (4530) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Drug Eruptions [MESH:D003875] (2697) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Erythema [MESH:D004890] (1330) 
 Erythema Multiforme [MESH:D004892] (1185) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Hair Diseases [MESH:D006201] (1891) 
 Hypotrichosis [MESH:D007039] (1513) 
 Alopecia [MESH:D000505] (1453)
 Pigmentation Disorders [MESH:D010859] (1215) 
 Hyperpigmentation [MESH:D017495] (523) 
 Melanosis [MESH:D008548] (459) 
 Lentigo [MESH:D007911] (329) 
 LEOPARD Syndrome [MESH:D044542] (299)
 Hypopigmentation [MESH:D017496] (718) 
 Vitiligo [MESH:D014820] (504)
 Skin Abnormalities [MESH:D012868] (1709) 
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Skin Diseases, Eczematous [MESH:D017443] (3740) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Skin Diseases, Genetic [MESH:D012873] (3481) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
 Hereditary Autoinflammatory Diseases [MESH:D056660] (247) 
 Periodic fever, familial, autosomal dominant [MESH:C536657] (177)
 Skin Diseases, Infectious [MESH:D012874] (2684) 
 Dermatomycoses [MESH:D003881] (267) 
 Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)
 Skin Diseases, Parasitic [MESH:D012876] (2526) 
 Leishmaniasis [MESH:D007896] (2516) 
 Leishmaniasis, Cutaneous [MESH:D016773] (2359) 
 Leishmaniasis, Mucocutaneous [MESH:D007897] (606)
 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)
 Skin Diseases, Vesiculobullous [MESH:D012872] (1754) 
 Pemphigoid, Bullous [MESH:D010391] (707)
 Erythema Multiforme [MESH:D004892] (1185) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
C18. Nutritional and Metabolic Diseases 
C18. Nutritional and Metabolic Diseases
 Metabolic Diseases [MESH:D008659] (9025) 
 Metabolic Syndrome X [MESH:D024821] (2151)
 Acid-Base Imbalance [MESH:D000137] (854) 
 Alkalosis [MESH:D000471] (384)
 Brain Diseases, Metabolic [MESH:D001928] (3350) 
 Hepatic Encephalopathy [MESH:D006501] (1795)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Peroxisomal Disorders [MESH:D018901] (1472) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Calcium Metabolism Disorders [MESH:D002128] (3634) 
 Hypercalcemia [MESH:D006934] (1999)
 Calcinosis [MESH:D002114] (2989) 
 Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)
 Aortic Valve, Calcification of [MESH:C562942] (655)
 DNA Repair-Deficiency Disorders [MESH:D049914] (2245) 
 Fanconi Anemia [MESH:D005199] (1604)
 Li-Fraumeni Syndrome [MESH:D016864] (859)
 Glucose Metabolism Disorders [MESH:D044882] (6122) 
 Hyperglycemia [MESH:D006943] (1858)
 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)
 Diabetes, Gestational [MESH:D016640] (1152)
 Hyperinsulinism [MESH:D006946] (3586) 
 Insulin Resistance [MESH:D007333] (3511) 
 Metabolic Syndrome X [MESH:D024821] (2151)
 Iron Metabolism Disorders [MESH:D019189] (2139) 
 Iron Overload [MESH:D019190] (1772) 
 Hemochromatosis [MESH:D006432] (1694)
 Lipid Metabolism Disorders [MESH:D052439] (3225) 
 Lipomatosis [MESH:D008068] (182)
 Dyslipidemias [MESH:D050171] (2428) 
 Hyperlipidemias [MESH:D006949] (1908) 
 Hypercholesterolemia [MESH:D006937] (1404)
 Hyperlipidemia, Familial Combined [MESH:D006950] (372)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (461) 
 Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)
 Lipidoses [MESH:D008064] (1655) 
 Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026) 
 Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)
 Malabsorption Syndromes [MESH:D008286] (1869) 
 Hyperhomocysteinemia [MESH:D020138] (1716)
 Metabolism, Inborn Errors [MESH:D008661] (6028) 
 Myeloperoxidase Deficiency [MESH:C562864] (335)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559) 
 Methylmalonic acidemia [MESH:C537358] (764)
 Hyperhomocysteinemia [MESH:D020138] (1724)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Peroxisomal Disorders [MESH:D018901] (1472) 
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)
 Hyperlipidemia, Familial Combined [MESH:D006950] (372)
 Lipidoses [MESH:D008064] (1655) 
 Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026) 
 Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)
 Metal Metabolism, Inborn Errors [MESH:D008664] (2017) 
 Hemochromatosis [MESH:D006432] (1694)
 Peroxisomal Disorders [MESH:D018901] (1788) 
 Acatalasia [MESH:D020642] (788)
 Adrenoleukodystrophy [MESH:D000326] (1348)
 Mitochondrial Diseases [MESH:D028361] (2561) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Mitochondrial Myopathies [MESH:D017240] (2176) 
 Mitochondrial Encephalomyopathies [MESH:D017237] (1121) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Proteostasis Deficiencies [MESH:D057165] (3522) 
 TDP-43 Proteinopathies [MESH:D057177] (3337) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Wasting Syndrome [MESH:D019282] (1959) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Water-Electrolyte Imbalance [MESH:D014883] (2790) 
 Hypercalcemia [MESH:D006934] (1999)
 Hypokalemia [MESH:D007008] (1041)
 Hyponatremia [MESH:D007010] (789)
 Nutrition Disorders [MESH:D009748] (4945) 
 Malnutrition [MESH:D044342] (2754) 
 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)
 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)
 Diabetes Mellitus [MESH:D003920] (6159) 
 Diabetes, Gestational [MESH:D016640] (1152)
 Diabetes Mellitus, Experimental [MESH:D003921] (4771)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
 Diabetes Mellitus, Type 2 [MESH:D003924] (4219)
 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)
 Dwarfism [MESH:D004392] (698) 
 Kniest dysplasia [MESH:C537207] (89)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Ovarian Neoplasms [MESH:D010051] (3275)
 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)
 Pancreatic Neoplasms [MESH:D010190] (3820) 
 Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)
 Thyroid Neoplasms [MESH:D013964] (2040) 
 Thyroid cancer, anaplastic [MESH:C536910] (489)
 Gonadal Disorders [MESH:D006058] (5088) 
 Puberty, Precocious [MESH:D011629] (1147)
 Testicular Diseases [MESH:D013733] (777)
 Ovarian Diseases [MESH:D010049] (4253) 
 Ovarian Neoplasms [MESH:D010051] (3281)
 Parathyroid Diseases [MESH:D010279] (1604) 
 Hyperparathyroidism [MESH:D006961] (1475) 
 Hyperparathyroidism, Secondary [MESH:D006962] (1138)
 Pituitary Diseases [MESH:D010900] (1829) 
 Pituitary Neoplasms [MESH:D010911] (981)
 Hyperpituitarism [MESH:D006964] (1259) 
 Acromegaly [MESH:D000172] (466)
 Thyroid Diseases [MESH:D013959] (2808) 
 Hyperthyroidism [MESH:D006980] (1191)
 Thyroid Neoplasms [MESH:D013964] (2040) 
 Thyroid cancer, anaplastic [MESH:C536910] (489)
C20. Immune System Diseases 
C20. Immune System Diseases
 Immune System Diseases [MESH:D007154] (7674) 
 Graft vs Host Disease [MESH:D006086] (674)
 Autoimmune Diseases [MESH:D001327] (5067) 
 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)
 Hepatitis, Autoimmune [MESH:D019693] (1982)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317)
 Pemphigoid, Bullous [MESH:D010391] (707)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810) 
 Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)
 Hypersensitivity [MESH:D006967] (5873) 
 Drug Hypersensitivity [MESH:D004342] (4000) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 Drug Eruptions [MESH:D003875] (2695) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Hypersensitivity, Delayed [MESH:D006968] (3408) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Hypersensitivity, Immediate [MESH:D006969] (4980) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 Dermatitis, Atopic [MESH:D003876] (2052)
 Urticaria [MESH:D014581] (2668)
 Respiratory Hypersensitivity [MESH:D012130] (4250) 
 Alveolitis, Extrinsic Allergic [MESH:D000542] (495)
 Asthma [MESH:D001249] (3914)
 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 Wasting Syndrome [MESH:D019247] (1956)
 Phagocyte Bactericidal Dysfunction [MESH:D010585] (999) 
 Granulomatous Disease, Chronic [MESH:D006105] (404) 
 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142)
 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) 
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Lymphoma, T-Cell [MESH:D016399] (1382) 
 Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)
 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)
 Cattle Diseases [MESH:D002418] (416) 
 Tuberculosis, Bovine [MESH:D014380] (380)
C23. Pathological Conditions, Signs and Symptoms 
C23. Pathological Conditions, Signs and Symptoms
 Pathological Conditions, Anatomical [MESH:D020763] (6074) 
 Alopecia [MESH:D000505] (1383)
 Plaque, Atherosclerotic [MESH:D058226] (696)
 Atrophy [MESH:D001284] (2603) 
 Muscular Atrophy [MESH:D009133] (1234)
 Hernia [MESH:D006547] (2825) 
 Hernia, Diaphragmatic [MESH:D006548] (2647)
 Hypertrophy [MESH:D006984] (4476) 
 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)
 Pathologic Processes [MESH:D010335] (9863) 
 Emphysema [MESH:D004646] (1096)
 Fibrosis [MESH:D005355] (3133)
 Gliosis [MESH:D005911] (1419)
 Hyperbilirubinemia [MESH:D006932] (1860)
 Hyperplasia [MESH:D006965] (2463)
 Ischemia [MESH:D007511] (3049)
 Leukocytosis [MESH:D007964] (978)
 Neointima [MESH:D058426] (814)
 Nerve Degeneration [MESH:D009410] (4061)
 Arrhythmias, Cardiac [MESH:D001145] (4658) 
 Atrial Fibrillation [MESH:D001281] (1053)
 Bradycardia [MESH:D001919] (1899)
 Long QT Syndrome [MESH:D008133] (691)
 Cardiac Complexes, Premature [MESH:D005117] (429) 
 Ventricular Premature Complexes [MESH:D018879] (418)
 Tachycardia [MESH:D013610] (3339) 
 Tachycardia, Ventricular [MESH:D017180] (1386)
 Chromosome Aberrations [MESH:D002869] (2352) 
 Aneuploidy [MESH:D000782] (1237) 
 Monosomy [MESH:D009006] (1121) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Death [MESH:D003643] (1328) 
 Death, Sudden [MESH:D003645] (725)
 Disease Attributes [MESH:D020969] (3654) 
 Disease Progression [MESH:D018450] (2868)
 Disease Susceptibility [MESH:D004198] (1200) 
 Genetic Predisposition to Disease [MESH:D020022] (966)
 Facies [MESH:D019066] (738) 
 Macrocephaly Autism Syndrome [MESH:C565342] (151)
 Granuloma [MESH:D006099] (587) 
 Granuloma, Respiratory Tract [MESH:D015769] (502)
 Growth Disorders [MESH:D006130] (2438) 
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Fetal Growth Retardation [MESH:D005317] (986)
 Hemorrhage [MESH:D006470] (4451) 
 Shock, Hemorrhagic [MESH:D012771] (2042)
 Gastrointestinal Hemorrhage [MESH:D006471] (815) 
 Peptic Ulcer Hemorrhage [MESH:D010438] (553)
 Intracranial Hemorrhages [MESH:D020300] (3241) 
 Cerebral Hemorrhage [MESH:D002543] (2872)
 Subarachnoid Hemorrhage [MESH:D013345] (1081)
 Purpura [MESH:D011693] (475) 
 Purpura, Thrombocytopenic [MESH:D011696] (237) 
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Inflammation [MESH:D007249] (5241) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Systemic Inflammatory Response Syndrome [MESH:D018746] (3563) 
 Sepsis [MESH:D018805] (3562) 
 Shock, Septic [MESH:D012772] (1830)
 Bacteremia [MESH:D016470] (1369) 
 Endotoxemia [MESH:D019446] (1289)
 Metaplasia [MESH:D008679] (1469) 
 Neovascularization, Pathologic [MESH:D009389] (829) 
 Choroidal Neovascularization [MESH:D020256] (550)
 Necrosis [MESH:D009336] (4019) 
 Osteonecrosis [MESH:D010020] (537) 
 Femur Head Necrosis [MESH:D005271] (266)
 Neoplastic Processes [MESH:D009385] (5317) 
 Neoplasm Invasiveness [MESH:D009361] (3388)
 Neoplasm Recurrence, Local [MESH:D009364] (1949)
 Neoplasm, Residual [MESH:D018365] (478)
 Carcinogenesis [MESH:D063646] (3391) 
 Cell Transformation, Neoplastic [MESH:D002471] (3389)
 Neoplasm Metastasis [MESH:D009362] (4441) 
 Lymphatic Metastasis [MESH:D008207] (917)
 Postoperative Complications [MESH:D011183] (5311) 
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Shock [MESH:D012769] (2550) 
 Multiple Organ Failure [MESH:D009102] (1836)
 Shock, Hemorrhagic [MESH:D012771] (2042)
 Systemic Inflammatory Response Syndrome [MESH:D018746] (1832) 
 Shock, Septic [MESH:D012772] (1830)
 Signs and Symptoms [MESH:D012816] (10659) 
 Asthenia [MESH:D001247] (376)
 Chills [MESH:D023341] (644)
 Edema [MESH:D004487] (3726)
 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)
 Neurologic Manifestations [MESH:D009461] (8702) 
 Reflex, Abnormal [MESH:D012021] (485)
 Seizures [MESH:D012640] (4502)
 Sleep Disorders [MESH:D012893] (1301)
 Dyskinesias [MESH:D020820] (3285) 
 Catalepsy [MESH:D002375] (1429)
 Hyperkinesis [MESH:D006948] (1799)
 Neurobehavioral Manifestations [MESH:D019954] (4706) 
 Lethargy [MESH:D053609] (1035)
 Intellectual Disability [MESH:D008607] (1476)
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Language Disorders [MESH:D007806] (653) 
 Language Development Disorders [MESH:D007805] (351)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Muscular Atrophy [MESH:D009133] (1234)
 Pain [MESH:D010146] (3869) 
 Headache [MESH:D006261] (1417)
 Pain, Intractable [MESH:D010148] (707)
 Back Pain [MESH:D001416] (285) 
 Low Back Pain [MESH:D017116] (244)
 Neuralgia [MESH:D009437] (2074) 
 Neuralgia, Postherpetic [MESH:D051474] (742)
 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) 
 Hearing Loss, Conductive [MESH:D006314] (134) 
 Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)
 Hearing Loss, Sensorineural [MESH:D006319] (1227) 
 Stickler syndrome, type 1 [MESH:C537492] (89)
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Somatosensory Disorders [MESH:D020886] (4000) 
 Hyperalgesia [MESH:D006930] (3929)
 Pain [MESH:D010146] (4511) 
 Headache [MESH:D006261] (1417)
 Pain, Intractable [MESH:D010148] (707)
 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, Unstable [MESH:D000789] (782)
 Angina, Stable [MESH:D060050] (1702)
 Neuralgia [MESH:D009437] (2074) 
 Neuralgia, Postherpetic [MESH:D051474] (742)
 Signs and Symptoms, Digestive [MESH:D012817] (3095) 
 Anorexia [MESH:D000855] (854)
 Nausea [MESH:D009325] (2300)
 Vomiting [MESH:D014839] (1354)
 Signs and Symptoms, Respiratory [MESH:D012818] (2724) 
 Anoxia [MESH:D000860] (1698)
 Hyperoxia [MESH:D018496] (694)
 Respiratory Sounds [MESH:D012135] (713)
 Skin Manifestations [MESH:D012877] (1250) 
 Purpura [MESH:D011693] (475) 
 Purpura, Thrombocytopenic [MESH:D011696] (237) 
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Urological Manifestations [MESH:D020924] (3532) 
 Polyuria [MESH:D011141] (279)
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
C24. Occupational Diseases 
C24. Occupational Diseases
 Z. Exceptions (1530) 
 Not Fully Specified [NFS] (1530)
 Occupational Diseases [MESH:D009784] (3402) 
 Pneumoconiosis [MESH:D011009] (2670) 
 Asbestosis [MESH:D001195] (935)
 Berylliosis [MESH:D001607] (2005)
 Silicosis [MESH:D012829] (1273)
C25. Chemically-Induced Disorders 
C25. Chemically-Induced Disorders
 Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839) 
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Drug Hypersensitivity [MESH:D004342] (4001) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 Drug Eruptions [MESH:D003875] (2697) 
 Stevens-Johnson Syndrome [MESH:D013262] (1163)
 Poisoning [MESH:D011041] (6703) 
 Arsenic Poisoning [MESH:D020261] (2540)
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Manganese Poisoning [MESH:D020149] (2214)
 Psychoses, Substance-Induced [MESH:D011605] (2053)
 Neurotoxicity Syndromes [MESH:D020258] (3323) 
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Substance-Related Disorders [MESH:D019966] (6308) 
 Amphetamine-Related Disorders [MESH:D019969] (2858)
 Cocaine-Related Disorders [MESH:D019970] (3054)
 Drug Overdose [MESH:D062787] (513)
 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) 
 Cardiomyopathy, Alcoholic [MESH:D002310] (354)
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 Hepatitis, Alcoholic [MESH:D006519] (1613)
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Opioid-Related Disorders [MESH:D009293] (1491) 
 Heroin Dependence [MESH:D006556] (950)
C26. Wounds and Injuries 
C26. Wounds and Injuries
 Z. Exceptions (2454) 
 Not Fully Specified [NFS] (2454)
 Wounds and Injuries [MESH:D014947] (5171) 
 Burns [MESH:D002056] (2565)
 Vascular System Injuries [MESH:D057772] (2086)
 Craniocerebral Trauma [MESH:D006259] (3523) 
 Brain Injuries [MESH:D001930] (3431)
 Radiation Injuries [MESH:D011832] (2718) 
 Radiation Injuries, Experimental [MESH:D011833] (2662)
 Spinal Cord Injuries [MESH:D013119] (2688) 
 Spinal Cord Compression [MESH:D013117] (1800)
 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)
D03. Heterocyclic Compounds 
D03. Heterocyclic Compounds
 Heterocyclic Compounds [MESH:D006571] (56330) 
 Heterocyclic Compounds, 1-Ring [MESH:D006573] (30631) 
 Azoles [MESH:D001393] (10398) 
 Pyrroles [MESH:D011758] (2361) 
 Tetrapyrroles [MESH:D045725] (1116) 
 Porphyrins [MESH:D011166] (952) 
 Protoporphyrins [MESH:D011524] (37)
 Heterocyclic Compounds with 4 or More Rings [MESH:D006576] (2763) 
 Tetrapyrroles [MESH:D045725] (1116) 
 Porphyrins [MESH:D011166] (952) 
 Protoporphyrins [MESH:D011524] (37)
D04. Polycyclic Compounds 
D04. Polycyclic Compounds
 Polycyclic Compounds [MESH:D011083] (22048) 
 Macrocyclic Compounds [MESH:D047028] (4784) 
 Tetrapyrroles [MESH:D045725] (1116) 
 Porphyrins [MESH:D011166] (952) 
 Protoporphyrins [MESH:D011524] (37)
D23. Biological Factors 
D23. Biological Factors
 Biological Factors [MESH:D001685] (12003) 
 Pigments, Biological [MESH:D010860] (2018) 
 Porphyrins [MESH:D011166] (942) 
 Protoporphyrins [MESH:D011524] (37)
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment 
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment
 Diagnosis [MESH:D003933] (1924) 
 Diagnostic Techniques and Procedures [MESH:D019937] (1902) 
 Physical Examination [MESH:D010808] (1041) 
 Facies [MESH:D019066] (704) 
 Macrocephaly Autism Syndrome [MESH:C565342] (151)
F. Psychiatry and Psychology 
F. Psychiatry and Psychology
 Mental Disorders [MESH:D001523] (2063) 
 Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245) 
 Child Development Disorders, Pervasive [MESH:D002659] (157) 
 Autistic Disorder [MESH:D001321] (154) 
 Macrocephaly Autism Syndrome [MESH:C565342] (151)
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)