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 4-oxoretinoic acid
C002202
 
  
  
  

MeSH Unique Identifier: C002202
Chemical – Gene Interaction

Note 1: 4-oxoretinoic acid results in decreased expression of AIP mRNA

Note 2: 4-oxoretinoic acid results in increased expression of ANXA1 mRNA

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1. Human Genes 
1. Human Genes
 Cadherins [HGNC:CDH] (214) 
 Cadherins, major [HGNC:MCDH] (189) 
 cadherin 1, type 1, E-cadherin (epithelial) [HGNC:CDH1] (122)
 desmocollin 1 [HGNC:DSC1] (12)
 S100 calcium binding proteins [HGNC:S100] (110) 
 S100 calcium binding protein A01 [HGNC:S100A1] (10)
 S100 calcium binding protein A07 [HGNC:S100A7] (9)
 S100 calcium binding protein A08 [HGNC:S100A8] (31)
 S100 calcium binding protein A09 [HGNC:S100A9] (33)
 CD molecules [HGNC:CD] (1459) 
 cadherin 01, type 1, E-cadherin (epithelial) [HGNC:CDH1] (122)
 integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor) [HGNC:ITGA4] (22)
 interleukin 10 receptor, alpha [HGNC:IL10RA] (14)
 Collagens [HGNC:COL] (230) 
 collagen, type I, alpha 1 [HGNC:COL1A1] (123)
 collagen, type IV, alpha 2 [HGNC:COL4A2] (26)
 collagen, type VI, alpha 1 [HGNC:COL6A1] (28)
 collagen, type VIII, alpha 2 [HGNC:COL8A2] (11)
 C-type lectin domain containing [HGNC:CLEC] (81) 
 oxidized low density lipoprotein (lectin-like) receptor 1 [HGNC:OLR1] (40)
 Cytochrome P450s [HGNC:CYP] (1673) 
 cytochrome P450, family 26, subfamily A, polypeptide 01 [HGNC:CYP26A1] (32)
 cytochrome P450, family 27, subfamily A, polypeptide 01 [HGNC:CYP27A1] (34)
 EF-hand domain containing [HGNC:EFHAND] (226) 
 filaggrin [HGNC:FLG] (11)
 S100 calcium binding protein A01 [HGNC:S100A1] (10)
 S100 calcium binding protein A07 [HGNC:S100A7] (9)
 S100 calcium binding protein A08 [HGNC:S100A8] (31)
 S100 calcium binding protein A09 [HGNC:S100A9] (33)
 Endogenous Ligands [HGNC:ENDOLIG] (1191) 
 chemokine (C-X-C motif) ligand 01 (melanoma growth stimulating activity, alpha) [HGNC:CXCL1] (82)
 Fatty acid binding protein family [HGNC:FABP] (151) 
 cellular retinoic acid binding protein 2 [HGNC:CRABP2] (32)
 fatty acid binding protein 5 (psoriasis-associated) [HGNC:FABP5] (29)
 Forkhead boxes [HGNC:FOX] (139) 
 forkhead box A1 [HGNC:FOXA1] (30)
 GATA zinc finger domain containing [HGNC:GATAD] (101) 
 GATA binding protein 6 [HGNC:GATA6] (38)
 Glutathione S-transferases [HGNC:GST] (460) 
 Glutathione S-transferases, soluble [HGNC:SGST] (447) 
 glutathione S-transferase mu 1 [HGNC:GSTM1] (144)
 Homeoboxes [HGNC:homeobox] (219) 
 Homeoboxes, ANTP class [HGNC:HOXL] (152) 
 HOXL subclass homeoboxes [HGNC:HOXL] (95) 
 mesenchyme homeobox 1 [HGNC:MEOX1] (14)
 Homeoboxes, TALE class [HGNC:TALE] (72) 
 Meis homeobox 1 [HGNC:MEIS1] (13)
 Integrins [HGNC:ITG] (284) 
 integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor) [HGNC:ITGA4] (22)
 Interleukins and interleukin receptors [HGNC:IL] (1294) 
 interleukin 01, beta [HGNC:IL1B] (497)
 interleukin 10 receptor, alpha [HGNC:IL10RA] (14)
 interleukin 24 [HGNC:IL24] (37)
 Intermediate filaments [HGNC:IF] (273) 
 Type I. Keratins (acidic) [HGNC:] (120) 
 keratin 10 [HGNC:KRT10] (27)
 keratin 14 [HGNC:KRT14] (13)
 keratin 15 [HGNC:KRT15] (23)
 keratin 17 [HGNC:KRT17] (36)
 keratin 18 [HGNC:KRT18] (50)
 keratin 19 [HGNC:KRT19] (40)
 Type II. Keratins (basic) [HGNC:] (106) 
 keratin 01 [HGNC:KRT1] (24)
 keratin 05 [HGNC:KRT5] (25)
 keratin 06A [HGNC:KRT6A] (18)
 keratin 07 [HGNC:KRT7] (30)
 keratin 08 [HGNC:KRT8] (53)
 keratin 75 [HGNC:KRT75] (10)
 Type IV [HGNC:] (57) 
 neurofilament, light polypeptide [HGNC:NEFL] (22)
 Keratins [HGNC:KRT] (161) 
 keratin 01 [HGNC:KRT1] (24)
 keratin 05 [HGNC:KRT5] (25)
 keratin 06A [HGNC:KRT6A] (18)
 keratin 07 [HGNC:KRT7] (30)
 keratin 08 [HGNC:KRT8] (53)
 keratin 10 [HGNC:KRT10] (27)
 keratin 14 [HGNC:KRT14] (13)
 keratin 15 [HGNC:KRT15] (23)
 keratin 17 [HGNC:KRT17] (36)
 keratin 18 [HGNC:KRT18] (50)
 keratin 19 [HGNC:KRT19] (40)
 keratin 75 [HGNC:KRT75] (10)
 Laminins [HGNC:LAM] (93) 
 laminin, alpha 2 [HGNC:LAMA2] (11)
 laminin, alpha 3 [HGNC:LAMA3] (25)
 laminin, gamma 3 [HGNC:LAMC3] (6)
 Low density lipoprotein receptors [HGNC:LDLR] (71) 
 lipocalin 2 [HGNC:LCN2] (25)
 Nuclear hormone receptors [HGNC:NR] (1322) 
 retinoic acid receptor, alpha [HGNC:RARA] (73)
 retinoic acid receptor, beta [HGNC:RARB] (56)
 Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227) 
 growth factor receptor-bound protein 07 [HGNC:GRB7] (16)
 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 : MAP kinase phosphatases [HGNC:DUSPT] (127) 
 dual specificity phosphatase 10 [HGNC:DUSP10] (34)
 Serine (or cysteine) peptidase inhibitors [HGNC:SERPIN] (252) 
 serpin peptidase inhibitor, clade B (ovalbumin), member 02 [HGNC:SERPINB2] (63)
 serpin peptidase inhibitor, clade B (ovalbumin), member 09 [HGNC:SERPINB9] (27)
 SH2 domain containing [HGNC:SH2D] (431) 
 growth factor receptor-bound protein 07 [HGNC:GRB7] (16)
 suppressor of cytokine signaling 1 [HGNC:SOCS1] (25)
 suppressor of cytokine signaling 2 [HGNC:SOCS2] (31)
 Short chain dehydrogenase/reductase superfamily [HGNC:SDR] (302) 
 Short chain dehydrogenase/reductase superfamily, Atypical [HGNC:SDRA] (89) 
 fatty acid synthase [HGNC:FASN] (72)
 Solute carriers [HGNC:SLC] (716) 
 solute carrier family 16 (monocarboxylate transporter), member 1 [HGNC:SLC16A1] (43)
 Sulfotransferases, cytosolic [HGNC:SULT] (167) 
 sulfotransferase family, cytosolic, 2A, dehydroepiandrosterone (DHEA)-preferring, member 1 [HGNC:SULT2A1] (47)
 Suppressors of cytokine signaling [HGNC:SOCS] (82) 
 suppressor of cytokine signaling 1 [HGNC:SOCS1] (25)
 suppressor of cytokine signaling 2 [HGNC:SOCS2] (31)
 Transglutaminases [HGNC:TGM] (82) 
 transglutaminase 1 [HGNC:TGM1] (15)
 transglutaminase 2 [HGNC:TGM2] (60)
2. Interaction: Human Genes and Chemicals 
2. Interaction: Human Genes and Chemicals
 Affects (3990) 
 expression (494)
 Decreases (5154) 
 expression (2187)
 Increases (5571) 
 chemical synthesis (464)
 expression (3238)
C01. Bacterial Infections and Mycoses 
C01. Bacterial Infections and Mycoses
 Bacterial Infections [MESH:D001424] (3716) 
 Bacteremia [MESH:D016470] (208)
 Gram-Negative Bacterial Infections [MESH:D016905] (3085) 
 Helicobacter Infections [MESH:D016481] (579)
 Mycoplasmatales Infections [MESH:D009180] (1949) 
 Mycoplasma Infections [MESH:D009175] (1947)
 Infection [MESH:D007239] (4109) 
 Sepsis [MESH:D018805] (3556) 
 Bacteremia [MESH:D016470] (1369)
C02. Virus Diseases 
C02. Virus Diseases
 Virus Diseases [MESH:D014777] (4544) 
 RNA Virus Infections [MESH:D012327] (4215) 
 Retroviridae Infections [MESH:D012192] (3420) 
 Lentivirus Infections [MESH:D016180] (3408) 
 HIV Infections [MESH:D015658] (3402) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Sexually Transmitted Diseases [MESH:D012749] (3305) 
 Sexually Transmitted Diseases, Viral [MESH:D015229] (3304) 
 HIV Infections [MESH:D015658] (3296) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
C03. Parasitic Diseases 
C03. Parasitic Diseases
 Parasitic Diseases [MESH:D010272] (3828) 
 Protozoan Infections [MESH:D011528] (3014) 
 Amebiasis [MESH:D000562] (1711) 
 Entamoebiasis [MESH:D004749] (1689)
 Euglenozoa Infections [MESH:D056986] (2552) 
 Leishmaniasis [MESH:D007896] (2541) 
 Leishmaniasis, Cutaneous [MESH:D016773] (2359)
 Leishmaniasis, Visceral [MESH:D007898] (2149)
 Malaria [MESH:D008288] (2175) 
 Malaria, Falciparum [MESH:D016778] (438)
 Skin Diseases, Parasitic [MESH:D012876] (2541) 
 Leishmaniasis [MESH:D007896] (2516) 
 Leishmaniasis, Cutaneous [MESH:D016773] (2359)
C04. Neoplasms 
C04. Neoplasms
 Neoplasms [MESH:D009369] (10293) 
 Neoplasms, Second Primary [MESH:D016609] (518)
 Cysts [MESH:D003560] (2625) 
 Ovarian Cysts [MESH:D010048] (2534)
 Neoplasms by Histologic Type [MESH:D009370] (8793) 
 Leukemia [MESH:D007938] (4576) 
 Leukemia, Lymphoid [MESH:D007945] (3047) 
 Leukemia, B-Cell [MESH:D015448] (2564) 
 Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
 Leukemia, Myeloid [MESH:D007951] (2773) 
 Leukemia, Myeloid, Acute [MESH:D015470] (2176) 
 Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)
 Lymphoma [MESH:D008223] (3686) 
 Lymphoma, Non-Hodgkin [MESH:D008228] (3337) 
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Lymphoma, T-Cell [MESH:D016399] (1405) 
 Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)
 Neoplasms, Complex and Mixed [MESH:D018193] (1121) 
 Wilms Tumor [MESH:D009396] (553)
 Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742) 
 Neoplasms, Adipose Tissue [MESH:D018205] (677) 
 Liposarcoma [MESH:D008080] (612)
 Neoplasms, Connective Tissue [MESH:D009372] (3626) 
 Neoplasms, Bone Tissue [MESH:D018213] (2217) 
 Osteosarcoma [MESH:D012516] (2175)
 Neoplasms, Muscle Tissue [MESH:D009379] (1965) 
 Leiomyosarcoma [MESH:D007890] (977)
 Myosarcoma [MESH:D009217] (790) 
 Rhabdomyosarcoma [MESH:D012208] (789)
 Sarcoma [MESH:D012509] (4246) 
 Hemangiosarcoma [MESH:D006394] (1836)
 Leiomyosarcoma [MESH:D007890] (977)
 Liposarcoma [MESH:D008080] (612)
 Osteosarcoma [MESH:D012516] (2175)
 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) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroendocrine Tumors [MESH:D018358] (3633) 
 Melanoma [MESH:D008545] (3508)
 Neoplasms, Glandular and Epithelial [MESH:D009375] (7760) 
 Adenoma [MESH:D000236] (4051) 
 ACTH-Secreting Pituitary Adenoma [MESH:D049913] (169)
 Adenoma, Oxyphilic [MESH:D018249] (115)
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Mesothelioma [MESH:D008654] (2567)
 Prolactinoma [MESH:D015175] (312)
 Adenomatous Polyps [MESH:D018256] (1571) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Carcinoma [MESH:D002277] (7263) 
 Carcinoma, Basal Cell [MESH:D002280] (1628)
 Carcinoma, Transitional Cell [MESH:D002295] (2662)
 Adenocarcinoma [MESH:D000230] (6565) 
 Adenocarcinoma of lung [MESH:C538231] (1487)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Adrenocortical Carcinoma [MESH:D018268] (821)
 Carcinoma, Adenoid Cystic [MESH:D003528] (1561)
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Carcinoma, Lobular [MESH:D018275] (305)
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Cholangiocarcinoma [MESH:D018281] (2398)
 Carcinoma, Ductal [MESH:D044584] (1786) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Carcinoma 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, Lobular [MESH:D018275] (305)
 Carcinoma, Ductal [MESH:D044584] (1786) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Neoplasms, Mesothelial [MESH:D018301] (2569) 
 Mesothelioma [MESH:D008654] (2567)
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neoplasms, Squamous Cell [MESH:D018307] (4457) 
 Papilloma [MESH:D010212] (2243)
 Carcinoma, Squamous Cell [MESH:D002294] (4294) 
 Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Neoplasms, Nerve Tissue [MESH:D009380] (5201) 
 Neuroectodermal Tumors [MESH:D017599] (5059) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroendocrine Tumors [MESH:D018358] (3625) 
 Melanoma [MESH:D008545] (3508)
 Neoplasms, Plasma Cell [MESH:D054219] (2772) 
 Multiple Myeloma [MESH:D009101] (2767)
 Neoplasms, Vascular Tissue [MESH:D009383] (2959) 
 Hemangiosarcoma [MESH:D006394] (1836)
 Nevi and Melanomas [MESH:D018326] (3572) 
 Melanoma [MESH:D008545] (3508)
 Neoplasms by Site [MESH:D009371] (9169) 
 Bone Neoplasms [MESH:D001859] (1334)
 Breast Neoplasms [MESH:D001943] (6077) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Digestive System Neoplasms [MESH:D004067] (7487) 
 Pancreatic Neoplasms [MESH:D010190] (3820)
 Biliary Tract Neoplasms [MESH:D001661] (1165) 
 Bile Duct Neoplasms [MESH:D001650] (367)
 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)
 Rectal Neoplasms [MESH:D012004] (717)
 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)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Ovarian Neoplasms [MESH:D010051] (3275)
 Pancreatic Neoplasms [MESH:D010190] (3820)
 Thyroid Neoplasms [MESH:D013964] (2040)
 Adrenal Gland Neoplasms [MESH:D000310] (917) 
 Adrenal Cortex Neoplasms [MESH:D000306] (823) 
 Adrenocortical Carcinoma [MESH:D018268] (821)
 Pituitary Neoplasms [MESH:D010911] (981) 
 ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Prolactinoma [MESH:D015175] (312)
 Head and Neck Neoplasms [MESH:D006258] (4612) 
 Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
 Thyroid Neoplasms [MESH:D013964] (2040)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Mouth Neoplasms [MESH:D009062] (2263) 
 Leukoplakia, Oral [MESH:D007972] (921)
 Salivary Gland Neoplasms [MESH:D012468] (968)
 Tongue Neoplasms [MESH:D014062] (1518)
 Otorhinolaryngologic Neoplasms [MESH:D010039] (1557) 
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Mammary Neoplasms, Animal [MESH:D015674] (3404) 
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 Nervous System Neoplasms [MESH:D009423] (3130) 
 Central Nervous System Neoplasms [MESH:D016543] (3055) 
 Brain Neoplasms [MESH:D001932] (2764) 
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Skin Neoplasms [MESH:D012878] (2992) 
 Dermatopathia pigmentosa reticularis [MESH:C535374] (38)
 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) 
 Uterine Neoplasms [MESH:D014594] (2431) 
 Endometrial Neoplasms [MESH:D016889] (1987)
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Prostatic Neoplasms [MESH:D011471] (6135) 
 Prostate cancer, familial [MESH:C537243] (264)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Wilms Tumor [MESH:D009396] (553)
 Neoplasms, Experimental [MESH:D009374] (5218) 
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 Neoplastic Processes [MESH:D009385] (5317) 
 Neoplasm Invasiveness [MESH:D009361] (3388)
 Neoplasm Recurrence, Local [MESH:D009364] (1949)
 Carcinogenesis [MESH:D063646] (3391) 
 Cell Transformation, Neoplastic [MESH:D002471] (3389)
 Neoplasm Metastasis [MESH:D009362] (4441) 
 Lymphatic Metastasis [MESH:D008207] (917)
 Neoplastic Syndromes, Hereditary [MESH:D009386] (2578) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Wilms Tumor [MESH:D009396] (553)
 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)
 Bone Diseases, Developmental [MESH:D001848] (3315) 
 Osteochondrodysplasias [MESH:D010009] (2440) 
 Hyperostosis, Cortical, Congenital [MESH:D006958] (392)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 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)
 Hyperostosis [MESH:D015576] (493) 
 Hyperostosis, Cortical, Congenital [MESH:D006958] (392)
 Spinal Diseases [MESH:D013122] (2485) 
 Ossification of Posterior Longitudinal Ligament [MESH:D017887] (99) 
 Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98)
 Joint Diseases [MESH:D007592] (4657) 
 Arthritis [MESH:D001168] (4416) 
 Arthritis, Experimental [MESH:D001169] (3142)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Osteoarthritis [MESH:D010003] (1743)
 Contracture [MESH:D003286] (296) 
 Bethlem myopathy [MESH:C535436] (108)
 Muscular Diseases [MESH:D009135] (4071) 
 Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)
 Contracture [MESH:D003286] (303) 
 Bethlem myopathy [MESH:C535436] (108)
 Mitochondrial Myopathies [MESH:D017240] (2176) 
 Mitochondrial Encephalomyopathies [MESH:D017237] (1121) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Muscular Disorders, Atrophic [MESH:D020966] (1598) 
 Muscular Dystrophies [MESH:D009136] (1593) 
 Bethlem myopathy [MESH:C535436] (108)
 Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 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) 
 Silver-Russell Syndrome [MESH:D056730] (142)
 Rheumatic Diseases [MESH:D012216] (4032) 
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Osteoarthritis [MESH:D010003] (1743)
C06. Digestive System Diseases 
C06. Digestive System Diseases
 Digestive System Diseases [MESH:D004066] (9461) 
 Biliary Tract Diseases [MESH:D001660] (3845) 
 Bile Duct Diseases [MESH:D001649] (3512) 
 Bile Duct Neoplasms [MESH:D001650] (367)
 Cholestasis [MESH:D002779] (3419) 
 Cholestasis, Intrahepatic [MESH:D002780] (1510) 
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 Biliary Tract Neoplasms [MESH:D001661] (1165) 
 Bile Duct Neoplasms [MESH:D001650] (367)
 Digestive System Abnormalities [MESH:D004065] (2127) 
 Barrett Esophagus [MESH:D001471] (1930)
 Digestive System Neoplasms [MESH:D004067] (7493) 
 Pancreatic Neoplasms [MESH:D010190] (3820)
 Biliary Tract Neoplasms [MESH:D001661] (1165) 
 Bile Duct Neoplasms [MESH:D001650] (367)
 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) 
 Rectal Neoplasms [MESH:D012004] (717)
 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)
 Gastrointestinal Diseases [MESH:D005767] (7443) 
 Esophageal Diseases [MESH:D004935] (4255) 
 Barrett Esophagus [MESH:D001471] (1930)
 Deglutition Disorders [MESH:D003680] (1538) 
 Esophageal Motility Disorders [MESH:D015154] (1489) 
 Gastroesophageal Reflux [MESH:D005764] (1465)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Gastroenteritis [MESH:D005759] (4066) 
 Mucositis [MESH:D052016] (1238)
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Enterocolitis [MESH:D004760] (1536) 
 Enterocolitis, Necrotizing [MESH:D020345] (1367)
 Gastritis [MESH:D005756] (967) 
 Gastritis, Atrophic [MESH:D005757] (947)
 Inflammatory Bowel Diseases [MESH:D015212] (3492) 
 Inflammatory Bowel Disease 28, Autosomal Recessive [MESH:C567728] (43)
 Colitis, Ulcerative [MESH:D003093] (2601)
 Crohn Disease [MESH:D003424] (2585)
 Gastrointestinal Neoplasms [MESH:D005770] (6460) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Intestinal Neoplasms [MESH:D007414] (5359) 
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Rectal Neoplasms [MESH:D012004] (717)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Intestinal Diseases [MESH:D007410] (6206) 
 Colonic Diseases [MESH:D003108] (5564) 
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Colorectal Neoplasms [MESH:D015179] (5282) 
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Duodenal Diseases [MESH:D004378] (1982) 
 Peptic Ulcer [MESH:D010437] (1969) 
 Duodenal Ulcer [MESH:D004381] (1549)
 Enterocolitis [MESH:D004760] (1536) 
 Enterocolitis, Necrotizing [MESH:D020345] (1367)
 Inflammatory Bowel Diseases [MESH:D015212] (3492) 
 Inflammatory Bowel Disease 28, Autosomal Recessive [MESH:C567728] (43)
 Colitis, Ulcerative [MESH:D003093] (2601)
 Crohn Disease [MESH:D003424] (2585)
 Intestinal Neoplasms [MESH:D007414] (5359) 
 Colorectal Neoplasms [MESH:D015179] (5294) 
 Rectal Neoplasms [MESH:D012004] (717)
 Colonic Neoplasms [MESH:D003110] (4405) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Intestinal Polyposis [MESH:D044483] (1610) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Malabsorption Syndromes [MESH:D008286] (492) 
 Celiac Disease [MESH:D002446] (340)
 Rectal Diseases [MESH:D012002] (4596) 
 Colorectal Neoplasms [MESH:D015179] (4534) 
 Rectal Neoplasms [MESH:D012004] (717)
 Peptic Ulcer [MESH:D010437] (3172) 
 Duodenal Ulcer [MESH:D004381] (1549)
 Stomach Ulcer [MESH:D013276] (2915)
 Stomach Diseases [MESH:D013272] (5325) 
 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)
 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) 
 Liver Failure, Acute [MESH:D017114] (2404)
 Hepatitis [MESH:D006505] (3883) 
 Hepatitis, Animal [MESH:D006520] (260)
 Hepatitis, Chronic [MESH:D006521] (2071) 
 Hepatitis, Autoimmune [MESH:D019693] (1982)
 Liver Cirrhosis [MESH:D008103] (5542) 
 Cirrhosis, Familial [MESH:C566123] (179)
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Liver Cirrhosis, Biliary [MESH:D008105] (1274)
 Liver Cirrhosis, Experimental [MESH:D008106] (4589)
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 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) 
 Pancreatic Neoplasms [MESH:D010190] (3820)
 Pancreatitis [MESH:D010195] (1924)
C07. Stomatognathic Diseases 
C07. Stomatognathic Diseases
 Stomatognathic Diseases [MESH:D009057] (5348) 
 Mouth Diseases [MESH:D009059] (4783) 
 Behcet Syndrome [MESH:D001528] (1784)
 Mucositis [MESH:D052016] (1238)
 Oral Submucous Fibrosis [MESH:D009914] (2432)
 Mouth Neoplasms [MESH:D009062] (2263) 
 Leukoplakia, Oral [MESH:D007972] (921)
 Salivary Gland Neoplasms [MESH:D012468] (968)
 Tongue Neoplasms [MESH:D014062] (1518)
 Salivary Gland Diseases [MESH:D012466] (1213) 
 Salivary Gland Neoplasms [MESH:D012468] (968)
 Tongue Diseases [MESH:D014060] (1544) 
 Tongue Neoplasms [MESH:D014062] (1518)
 Pharyngeal Diseases [MESH:D010608] (1562) 
 Nasopharyngeal Diseases [MESH:D009302] (1508) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
C08. Respiratory Tract Diseases 
C08. Respiratory Tract Diseases
 Respiratory Tract Diseases [MESH:D012140] (7881) 
 Bronchial Diseases [MESH:D001982] (4382) 
 Bronchial Hyperreactivity [MESH:D016535] (1357)
 Asthma [MESH:D001249] (4098) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 Laryngeal Diseases [MESH:D007818] (215) 
 Laryngo onycho cutaneous syndrome [MESH:C537032] (49)
 Lung Diseases [MESH:D008171] (7249) 
 Hypertension, Pulmonary [MESH:D006976] (2000)
 Pneumonia [MESH:D011014] (3482)
 Pulmonary Edema [MESH:D011654] (2109)
 Pulmonary Embolism [MESH:D011655] (1118)
 Pulmonary Fibrosis [MESH:D011658] (3140)
 Lung Diseases, Interstitial [MESH:D017563] (2966) 
 Pneumoconiosis [MESH:D011009] (2789) 
 Anthracosis [MESH:D055008] (1805)
 Lung Diseases, Obstructive [MESH:D008173] (4697) 
 Asthma [MESH:D001249] (3903)
 Lung Injury [MESH:D055370] (3688) 
 Acute Lung Injury [MESH:D055371] (1907)
 Pneumoconiosis [MESH:D011009] (2789) 
 Anthracosis [MESH:D055008] (1805)
 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)
 Pleural Diseases [MESH:D010995] (2240) 
 Pleurisy [MESH:D010998] (2070)
 Respiratory Hypersensitivity [MESH:D012130] (4401) 
 Asthma [MESH:D001249] (4098) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 Respiratory Tract Infections [MESH:D012141] (3926) 
 Pleurisy [MESH:D010998] (2070)
 Pneumonia [MESH:D011014] (3482)
 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, Sensorineural [MESH:D006319] (1227) 
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Laryngeal Diseases [MESH:D007818] (211) 
 Laryngo onycho cutaneous syndrome [MESH:C537032] (49)
 Otorhinolaryngologic Neoplasms [MESH:D010039] (1561) 
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Pharyngeal Diseases [MESH:D010608] (1605) 
 Nasopharyngeal Diseases [MESH:D009302] (1508) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
 Pharyngeal Neoplasms [MESH:D010610] (1520) 
 Nasopharyngeal Neoplasms [MESH:D009303] (1500)
C10. Nervous System Diseases 
C10. Nervous System Diseases
 Z. Exceptions (4027) 
 Not Fully Specified [NFS] (4027)
 Nervous System Diseases [MESH:D009422] (13325) 
 Restless Legs Syndrome [MESH:D012148] (379)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Myasthenia Gravis [MESH:D009157] (632)
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Central Nervous System Diseases [MESH:D002493] (9745) 
 Brain Diseases [MESH:D001927] (9294) 
 Brain Injuries [MESH:D001930] (3429)
 Basal Ganglia Diseases [MESH:D001480] (4268) 
 Parkinsonian Disorders [MESH:D020734] (4009) 
 Lewy Body Disease [MESH:D020961] (1143)
 Parkinson Disease [MESH:D010300] (3595)
 Brain Diseases, Metabolic [MESH:D001928] (3351) 
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Brain Neoplasms [MESH:D001932] (2764) 
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Cerebrovascular Disorders [MESH:D002561] (5542) 
 Vasospasm, Intracranial [MESH:D020301] (324)
 Brain Ischemia [MESH:D002545] (4873) 
 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) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Embolism and Thrombosis [MESH:D002542] (490) 
 Intracranial Thrombosis [MESH:D020767] (481)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (221) 
 Hematoma, Subdural [MESH:D006408] (212)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Dementia [MESH:D003704] (4498) 
 Alzheimer Disease [MESH:D000544] (4275)
 Lewy Body Disease [MESH:D020961] (1143)
 Encephalitis [MESH:D004660] (226) 
 Meningoencephalitis [MESH:D008590] (179)
 Epilepsy [MESH:D004827] (6274) 
 Seizures [MESH:D012640] (4502)
 Status Epilepticus [MESH:D013226] (4014)
 Epilepsies, Myoclonic [MESH:D004831] (1344) 
 Myoclonic Epilepsies, Progressive [MESH:D020191] (1101) 
 MERRF Syndrome [MESH:D017243] (1053)
 Epilepsy, Generalized [MESH:D004829] (1431) 
 Epilepsy, Tonic-Clonic [MESH:D004830] (1042)
 Hypothalamic Diseases [MESH:D007027] (1833) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Pituitary Diseases [MESH:D010900] (1808) 
 Hyperpituitarism [MESH:D006964] (1250) 
 Acromegaly [MESH:D000172] (466)
 Pituitary Neoplasms [MESH:D010911] (981) 
 ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Prolactinoma [MESH:D015175] (312)
 Central Nervous System Infections [MESH:D002494] (1823) 
 Meningoencephalitis [MESH:D008590] (207)
 Encephalitis [MESH:D004660] (351) 
 Meningoencephalitis [MESH:D008590] (179)
 Meningitis [MESH:D008581] (1506) 
 Meningoencephalitis [MESH:D008590] (179)
 Meningitis [MESH:D008581] (352) 
 Meningoencephalitis [MESH:D008590] (179)
 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)
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Cranial Nerve Diseases [MESH:D003389] (2004) 
 Ocular Motility Disorders [MESH:D015835] (1697) 
 Ophthalmoplegia [MESH:D009886] (1468) 
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Optic Nerve Diseases [MESH:D009901] (1375) 
 Optic Atrophy [MESH:D009896] (1203) 
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Demyelinating Diseases [MESH:D003711] (2917) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Nervous System Malformations [MESH:D009421] (3354) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Nervous System Neoplasms [MESH:D009423] (3073) 
 Central Nervous System Neoplasms [MESH:D016543] (3055) 
 Brain Neoplasms [MESH:D001932] (2764) 
 Supratentorial Neoplasms [MESH:D015173] (930) 
 Hypothalamic Neoplasms [MESH:D007029] (922) 
 Pituitary Neoplasms [MESH:D010911] (914)
 Neurodegenerative Diseases [MESH:D019636] (6613) 
 Lewy Body Disease [MESH:D020961] (1143)
 Parkinson Disease [MESH:D010300] (3595)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 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)
 Paresis [MESH:D010291] (419)
 Seizures [MESH:D012640] (4514)
 Dyskinesias [MESH:D020820] (3365) 
 Hypokinesia [MESH:D018476] (279)
 Neurobehavioral Manifestations [MESH:D019954] (5230) 
 Lethargy [MESH:D053609] (1035)
 Memory Disorders [MESH:D008569] (3233)
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Language Disorders [MESH:D007806] (653) 
 Speech Disorders [MESH:D013064] (482) 
 Aphasia [MESH:D001037] (219)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Muscular Atrophy [MESH:D009133] (1234)
 Pain [MESH:D010146] (3875) 
 Back Pain [MESH:D001416] (287) 
 Low Back Pain [MESH:D017116] (244)
 Paralysis [MESH:D010243] (2043) 
 Ophthalmoplegia [MESH:D009886] (1468) 
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)
 Sensation Disorders [MESH:D012678] (5011) 
 Taste Disorders [MESH:D013651] (461)
 Hearing Disorders [MESH:D006311] (2103) 
 Hearing Loss [MESH:D034381] (2068) 
 Hearing Loss, Sensorineural [MESH:D006319] (1227) 
 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) 
 Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)
 Muscular Disorders, Atrophic [MESH:D020966] (1594) 
 Muscular Dystrophies [MESH:D009136] (1589) 
 Bethlem myopathy [MESH:C535436] (108)
 Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Mitochondrial Myopathies [MESH:D017240] (2176) 
 Mitochondrial Encephalomyopathies [MESH:D017237] (1121) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Myositis [MESH:D009220] (2069) 
 Dermatomyositis [MESH:D003882] (1826)
 Polymyositis [MESH:D017285] (2007) 
 Dermatomyositis [MESH:D003882] (1826)
 Neuromuscular Junction Diseases [MESH:D020511] (712) 
 Myasthenia Gravis [MESH:D009157] (632)
 Peripheral Nervous System Diseases [MESH:D010523] (6151) 
 Diabetic Neuropathies [MESH:D003929] (2442)
 Mononeuropathies [MESH:D020422] (604) 
 Sciatic Neuropathy [MESH:D020426] (477)
 Polyneuropathies [MESH:D011115] (1134) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Neurotoxicity Syndromes [MESH:D020258] (4570) 
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912) 
 Arsenic Poisoning [MESH:D020261] (2540)
 Manganese Poisoning [MESH:D020149] (2214)
 Sleep Disorders [MESH:D012893] (2050) 
 Dyssomnias [MESH:D020920] (1417) 
 Sleep Deprivation [MESH:D012892] (233)
 Sleep Disorders, Intrinsic [MESH:D020919] (1270) 
 Restless Legs Syndrome [MESH:D012148] (379)
 Disorders of Excessive Somnolence [MESH:D006970] (581) 
 Narcolepsy [MESH:D009290] (478)
 Parasomnias [MESH:D020447] (453) 
 Restless Legs Syndrome [MESH:D012148] (379)
 Trauma, Nervous System [MESH:D020196] (3997) 
 Craniocerebral Trauma [MESH:D006259] (3507) 
 Brain Injuries [MESH:D001930] (3431)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (221) 
 Hematoma, Subdural [MESH:D006408] (212)
C11. Eye Diseases 
C11. Eye Diseases
 Eye Diseases [MESH:D005128] (6245) 
 Conjunctival Diseases [MESH:D003229] (273) 
 Laryngo onycho cutaneous syndrome [MESH:C537032] (49)
 Corneal Diseases [MESH:D003316] (1445) 
 Corneal Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Posterior Polymorphous, 1 [MESH:C562745] (25)
 Corneal Dystrophy, Posterior Polymorphous, 2 [MESH:C565176] (18)
 Fuchs' Endothelial Dystrophy [MESH:D005642] (86) 
 Corneal dystrophy, Fuchs' endothelial, 1 [MESH:C535478] (18)
 Eye Diseases, Hereditary [MESH:D015785] (1869) 
 Corneal Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Posterior Polymorphous, 1 [MESH:C562745] (25)
 Corneal Dystrophy, Posterior Polymorphous, 2 [MESH:C565176] (18)
 Fuchs' Endothelial Dystrophy [MESH:D005642] (86) 
 Corneal dystrophy, Fuchs' endothelial, 1 [MESH:C535478] (18)
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Lacrimal Apparatus Diseases [MESH:D007766] (644) 
 Dry Eye Syndromes [MESH:D015352] (533)
 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) 
 Myopia [MESH:D009216] (349)
 Retinal Diseases [MESH:D012164] (3747) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Retinal Degeneration [MESH:D012162] (2386) 
 Retinal Dystrophies [MESH:D058499] (1315) 
 Retinitis Pigmentosa [MESH:D012174] (1307) 
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Uveal Diseases [MESH:D014603] (2428) 
 Uveitis [MESH:D014605] (2157) 
 Panuveitis [MESH:D015864] (1805) 
 Uveitis, Anterior [MESH:D014606] (1791) 
 Behcet Syndrome [MESH:D001528] (1784)
C12. Male Urogenital Diseases 
C12. Male Urogenital Diseases
 Male Urogenital Diseases [MESH:D052801] (8891) 
 Genital Diseases, Male [MESH:D005832] (6794) 
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Prostatic Neoplasms [MESH:D011471] (6135) 
 Prostate cancer, familial [MESH:C537243] (264)
 Prostatic Diseases [MESH:D011469] (6204) 
 Prostatic Neoplasms [MESH:D011471] (6135) 
 Prostate cancer, familial [MESH:C537243] (264)
 Urogenital Neoplasms [MESH:D014565] (6932) 
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Prostatic Neoplasms [MESH:D011471] (6135) 
 Prostate cancer, familial [MESH:C537243] (264)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Wilms Tumor [MESH:D009396] (553)
 Urologic Diseases [MESH:D014570] (7792) 
 Kidney Diseases [MESH:D007674] (7242) 
 Hydronephrosis [MESH:D006869] (956)
 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)
 Wilms Tumor [MESH:D009396] (553)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758)
 Nephrosis [MESH:D009401] (2228) 
 Nephrotic Syndrome [MESH:D009404] (1536)
 Renal Insufficiency [MESH:D051437] (4951) 
 Acute Kidney Injury [MESH:D058186] (4142)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Uremia [MESH:D014511] (2898) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Urethral Diseases [MESH:D014522] (955) 
 Urethral Obstruction [MESH:D014524] (937) 
 Urinary Bladder Neck Obstruction [MESH:D001748] (924)
 Urinary Bladder Diseases [MESH:D001745] (4374) 
 Urinary Bladder Neck Obstruction [MESH:D001748] (924)
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Urination Disorders [MESH:D014555] (3598) 
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
C13. Female Urogenital Diseases and Pregnancy Complications 
C13. Female Urogenital Diseases and Pregnancy Complications
 Z. Exceptions (1116) 
 Not Fully Specified [NFS] (1116)
 Female Urogenital Diseases [MESH:D052776] (8724) 
 Genital Diseases, Female [MESH:D005831] (5563) 
 Endometriosis [MESH:D004715] (2461)
 Adnexal Diseases [MESH:D000291] (4273) 
 Ovarian Diseases [MESH:D010049] (4255) 
 Ovarian Cysts [MESH:D010048] (2534)
 Ovarian Neoplasms [MESH:D010051] (3281)
 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)
 Urogenital Neoplasms [MESH:D014565] (5792) 
 Genital Neoplasms, Female [MESH:D005833] (3810) 
 Ovarian Neoplasms [MESH:D010051] (3281)
 Uterine Neoplasms [MESH:D014594] (2433) 
 Endometrial Neoplasms [MESH:D016889] (1989)
 Uterine Cervical Neoplasms [MESH:D002583] (978)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Wilms Tumor [MESH:D009396] (553)
 Urologic Diseases [MESH:D014570] (7793) 
 Kidney Diseases [MESH:D007674] (7242) 
 Hydronephrosis [MESH:D006869] (956)
 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)
 Wilms Tumor [MESH:D009396] (553)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758)
 Nephrosis [MESH:D009401] (2228) 
 Nephrotic Syndrome [MESH:D009404] (1536)
 Renal Insufficiency [MESH:D051437] (4951) 
 Acute Kidney Injury [MESH:D058186] (4142)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Uremia [MESH:D014511] (2898) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Urethral Diseases [MESH:D014522] (955) 
 Urethral Obstruction [MESH:D014524] (937) 
 Urinary Bladder Neck Obstruction [MESH:D001748] (924)
 Urinary Bladder Diseases [MESH:D001745] (4375) 
 Urinary Bladder Neck Obstruction [MESH:D001748] (924)
 Urinary Bladder Neoplasms [MESH:D001749] (4079)
 Urination Disorders [MESH:D014555] (3598) 
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
 Pregnancy Complications [MESH:D011248] (4768) 
 Abortion, Spontaneous [MESH:D000022] (2780)
 Placenta Diseases [MESH:D010922] (1781)
 Polyhydramnios [MESH:D006831] (123)
 Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)
 Fetal Diseases [MESH:D005315] (1206) 
 Fetal Growth Retardation [MESH:D005317] (986)
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)
 Heart Diseases [MESH:D006331] (8614) 
 Arrhythmias, Cardiac [MESH:D001145] (4679)
 Cardiac Tamponade [MESH:D002305] (175)
 Heart Failure [MESH:D006333] (4058)
 Pericardial Effusion [MESH:D010490] (1015)
 Cardiomegaly [MESH:D006332] (4081) 
 Cardiomyopathy, Dilated [MESH:D002311] (1576)
 Hypertrophy, Left Ventricular [MESH:D017379] (1430)
 Cardiomyopathies [MESH:D009202] (5331) 
 Cardiomyopathy, Dilated [MESH:D002311] (1576)
 Diabetic Cardiomyopathies [MESH:D058065] (1995)
 Kearns-Sayre Syndrome [MESH:D007625] (1054)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Heart Valve Diseases [MESH:D006349] (3333) 
 Aortic Valve Insufficiency [MESH:D001022] (1002)
 Myocardial Ischemia [MESH:D017202] (5787) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Angina Pectoris [MESH:D000787] (2575) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Coronary Disease [MESH:D003327] (3439) 
 Coronary Artery Disease [MESH:D003324] (2685)
 Coronary Thrombosis [MESH:D003328] (255)
 Myocardial Infarction [MESH:D009203] (4122) 
 Shock, Cardiogenic [MESH:D012770] (269)
 Ventricular Dysfunction [MESH:D018754] (2348) 
 Ventricular Dysfunction, Left [MESH:D018487] (1631)
 Vascular Diseases [MESH:D014652] (8691) 
 Angioedema [MESH:D000799] (837)
 Hyperemia [MESH:D006940] (2372)
 Hypertension [MESH:D006973] (5655)
 Hypotension [MESH:D007022] (4045)
 Aneurysm [MESH:D000783] (1886) 
 Aneurysm, Dissecting [MESH:D000784] (699)
 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)
 Cerebrovascular Disorders [MESH:D002561] (5541) 
 Vasospasm, Intracranial [MESH:D020301] (324)
 Brain Ischemia [MESH:D002545] (4873) 
 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) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Intracranial Thrombosis [MESH:D020767] (481)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (221) 
 Hematoma, Subdural [MESH:D006408] (212)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Diabetic Angiopathies [MESH:D003925] (1984) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Embolism and Thrombosis [MESH:D016769] (3374) 
 Embolism [MESH:D004617] (1137) 
 Pulmonary Embolism [MESH:D011655] (1118)
 Embolism, Fat [MESH:D004620] (261) 
 Embolism, Cholesterol [MESH:D017700] (255)
 Thromboembolism [MESH:D013923] (732) 
 Venous Thromboembolism [MESH:D054556] (400)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Intracranial Thrombosis [MESH:D020767] (481)
 Thrombosis [MESH:D013927] (3101) 
 Coronary Thrombosis [MESH:D003328] (255)
 Venous Thrombosis [MESH:D020246] (1141)
 Thromboembolism [MESH:D013923] (732) 
 Venous Thromboembolism [MESH:D054556] (400)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Intracranial Thrombosis [MESH:D020767] (481)
 Hemostatic Disorders [MESH:D020141] (2894) 
 Multiple Myeloma [MESH:D009101] (2765)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Myocardial Ischemia [MESH:D017202] (5791) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Angina Pectoris [MESH:D000787] (2575) 
 Acute Coronary Syndrome [MESH:D054058] (2286)
 Coronary Disease [MESH:D003327] (3439) 
 Coronary Artery Disease [MESH:D003324] (2685)
 Coronary Thrombosis [MESH:D003328] (255)
 Myocardial Infarction [MESH:D009203] (4151) 
 Shock, Cardiogenic [MESH:D012770] (269)
 Peripheral Vascular Diseases [MESH:D016491] (1412) 
 Raynaud Disease [MESH:D011928] (490)
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Vasculitis [MESH:D014657] (2604) 
 Behcet Syndrome [MESH:D001528] (1784)
C15. Hemic and Lymphatic Diseases 
C15. Hemic and Lymphatic Diseases
 Z. Exceptions (453) 
 Not Fully Specified [NFS] (453)
 Hematologic Diseases [MESH:D006402] (6174) 
 Anemia [MESH:D000740] (3966) 
 Anemia, Sideroblastic [MESH:D000756] (636)
 Anemia, Hemolytic [MESH:D000743] (3083) 
 Favism [MESH:D005236] (193)
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Anemia, Hemolytic, Congenital [MESH:D000745] (2001) 
 Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)
 Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (196) 
 Favism [MESH:D005236] (193)
 Thalassemia [MESH:D013789] (501) 
 beta-Thalassemia [MESH:D017086] (458)
 Blood Platelet Disorders [MESH:D001791] (3174) 
 Thrombocytopenia [MESH:D013921] (2966) 
 Thrombotic Microangiopathies [MESH:D057049] (2598) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Blood Protein Disorders [MESH:D001796] (3051) 
 Paraproteinemias [MESH:D010265] (2781) 
 Multiple Myeloma [MESH:D009101] (2765)
 Bone Marrow Diseases [MESH:D001855] (2944) 
 Myelodysplastic Syndromes [MESH:D009190] (2093) 
 Anemia, Sideroblastic [MESH:D000756] (636)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Thalassemia [MESH:D013789] (511) 
 beta-Thalassemia [MESH:D017086] (458)
 Hemorrhagic Disorders [MESH:D006474] (3359) 
 Hemostatic Disorders [MESH:D020141] (2932) 
 Multiple Myeloma [MESH:D009101] (2765)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Leukocyte Disorders [MESH:D007960] (2662) 
 Leukocytosis [MESH:D007964] (988)
 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)
 Lymphatic Diseases [MESH:D008206] (5167) 
 Lymphoproliferative Disorders [MESH:D008232] (4638) 
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Leukemia, Lymphoid [MESH:D007945] (3047) 
 Leukemia, B-Cell [MESH:D015448] (2564) 
 Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
 Lymphoma [MESH:D008223] (3684) 
 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] (1204) 
 Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)
 Splenic Diseases [MESH:D013158] (1323) 
 Hypersplenism [MESH:D006971] (341)
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities 
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
 Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152) 
 Congenital Abnormalities [MESH:D000013] (8109) 
 Abnormalities, Drug-Induced [MESH:D000014] (1024)
 Abnormalities, Multiple [MESH:D000015] (3192) 
 Beckwith-Wiedemann Syndrome [MESH:D001506] (193)
 Silver-Russell Syndrome [MESH:D056730] (142)
 Ectodermal Dysplasia [MESH:D004476] (938) 
 Naegeli syndrome [MESH:C538331] (38)
 Chromosome Disorders [MESH:D025063] (2030) 
 Beckwith-Wiedemann Syndrome [MESH:D001506] (193)
 Silver-Russell Syndrome [MESH:D056730] (142)
 Musculoskeletal Abnormalities [MESH:D009139] (3779) 
 Craniofacial Abnormalities [MESH:D019465] (3064)
 Nervous System Malformations [MESH:D009421] (3354) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Skin Abnormalities [MESH:D012868] (1723) 
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Naegeli syndrome [MESH:C538331] (38)
 Pachyonychia Congenita [MESH:D053549] (80) 
 Steatocystoma Multiplex [MESH:D062685] (56)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Epidermolysis Bullosa Simplex [MESH:D016110] (140) 
 Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)
 Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)
 Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)
 Ichthyosis [MESH:D007057] (481) 
 Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)
 Ichthyosis Vulgaris [MESH:D016112] (27)
 Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238) 
 Hyperkeratosis, Epidermolytic [MESH:D017488] (136) 
 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)
 Ichthyosis, Lamellar [MESH:D017490] (81) 
 Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)
 Fetal Diseases [MESH:D005315] (1205) 
 Fetal Growth Retardation [MESH:D005317] (986)
 Genetic Diseases, Inborn [MESH:D030342] (9766) 
 Cirrhosis, Familial [MESH:C566123] (179)
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)
 Anemia, Hemolytic, Congenital [MESH:D000745] (2001) 
 Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)
 Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (196) 
 Favism [MESH:D005236] (193)
 Thalassemia [MESH:D013789] (501) 
 beta-Thalassemia [MESH:D017086] (458)
 Chromosome Disorders [MESH:D025063] (2030) 
 Beckwith-Wiedemann Syndrome [MESH:D001506] (193)
 Silver-Russell Syndrome [MESH:D056730] (142)
 Dwarfism [MESH:D004392] (783) 
 Silver-Russell Syndrome [MESH:D056730] (142)
 Eye Diseases, Hereditary [MESH:D015785] (1867) 
 Corneal Dystrophies, Hereditary [MESH:D003317] (341) 
 Corneal Dystrophy, Posterior Polymorphous, 1 [MESH:C562745] (25)
 Corneal Dystrophy, Posterior Polymorphous, 2 [MESH:C565176] (18)
 Fuchs' Endothelial Dystrophy [MESH:D005642] (86) 
 Corneal dystrophy, Fuchs' endothelial, 1 [MESH:C535478] (18)
 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)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Thalassemia [MESH:D013789] (511) 
 beta-Thalassemia [MESH:D017086] (458)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Optic Atrophies, Hereditary [MESH:D015418] (1151) 
 Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)
 Metabolism, Inborn Errors [MESH:D008661] (6032) 
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565) 
 Glutamine deficiency, congenital [MESH:C536832] (117)
 Methylmalonic acidemia [MESH:C537358] (764)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100) 
 Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (195)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)
 Lipidoses [MESH:D008064] (1655) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Lysosomal Storage Diseases [MESH:D016464] (761) 
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Peroxisomal Disorders [MESH:D018901] (1788) 
 Acatalasia [MESH:D020642] (788)
 Muscular Dystrophies [MESH:D009136] (1597) 
 Bethlem myopathy [MESH:C535436] (108)
 Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Neoplastic Syndromes, Hereditary [MESH:D009386] (2578) 
 Adenomatous Polyposis Coli [MESH:D011125] (1565)
 Wilms Tumor [MESH:D009396] (553)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 Skin Diseases, Genetic [MESH:D012873] (3456) 
 dowling-degos disease [MESH:C562924] (53)
 Ichthyosis Vulgaris [MESH:D016112] (27)
 Dermatitis, Atopic [MESH:D003876] (2052) 
 Dermatitis, Atopic, 2 [MESH:C565293] (26)
 Dermatitis, Atopic, 1 [MESH:C566404] (26)
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Naegeli syndrome [MESH:C538331] (38)
 Pachyonychia Congenita [MESH:D053549] (80) 
 Steatocystoma Multiplex [MESH:D062685] (56)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (259) 
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Epidermolysis Bullosa Simplex [MESH:D016110] (140) 
 Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)
 Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)
 Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)
 Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238) 
 Hyperkeratosis, Epidermolytic [MESH:D017488] (136) 
 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)
 Ichthyosis, Lamellar [MESH:D017490] (81) 
 Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)
 Keratoderma, Palmoplantar [MESH:D007645] (287) 
 Keratosis palmoplantaris striata 1 [MESH:C536162] (54)
 Keratosis palmoplantaris striata 3 [MESH:C536163] (48)
 Naegeli syndrome [MESH:C538331] (38)
 Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80) 
 Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)
 Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)
 Infant, Newborn, Diseases [MESH:D007232] (3064) 
 Asphyxia Neonatorum [MESH:D001238] (1648)
 Hyperostosis, Cortical, Congenital [MESH:D006958] (392)
 Ichthyosis [MESH:D007057] (476) 
 Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)
 Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238) 
 Hyperkeratosis, Epidermolytic [MESH:D017488] (136) 
 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)
 Ichthyosis, Lamellar [MESH:D017490] (81) 
 Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)
 Infant, Premature, Diseases [MESH:D007235] (1292) 
 Bronchopulmonary Dysplasia [MESH:D001997] (1021)
C17. Skin and Connective Tissue Diseases 
C17. Skin and Connective Tissue Diseases
 Connective Tissue Diseases [MESH:D003240] (4490) 
 Dermatomyositis [MESH:D003882] (1826)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317)
 Scleroderma, Systemic [MESH:D012595] (199)
 Collagen Diseases [MESH:D003095] (1267) 
 Keloid [MESH:D007627] (1111)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Osteogenesis Imperfecta [MESH:D010013] (481) 
 Osteogenesis imperfecta, type 2A [MESH:C536042] (375)
 Osteogenesis imperfecta, type 3 [MESH:C536044] (375)
 Osteogenesis imperfecta, type 4 [MESH:C536045] (375)
 Rheumatic Diseases [MESH:D012216] (3619) 
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Skin Diseases [MESH:D012871] (8774) 
 Dermatomyositis [MESH:D003882] (1826)
 Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)
 Scleroderma, Systemic [MESH:D012595] (199)
 Skin Ulcer [MESH:D012883] (229)
 Acneiform Eruptions [MESH:D017486] (1312) 
 Chloracne [MESH:D054506] (1274)
 Breast Diseases [MESH:D001941] (6148) 
 Breast Neoplasms [MESH:D001943] (6077) 
 Carcinoma, Ductal, Breast [MESH:D018270] (1112)
 Dermatitis [MESH:D003872] (4530) 
 Eczema [MESH:D004485] (235)
 Dermatitis, Atopic [MESH:D003876] (2052) 
 Dermatitis, Atopic, 2 [MESH:C565293] (26)
 Dermatitis, Atopic, 1 [MESH:C566404] (26)
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Dermatitis, Seborrheic [MESH:D012628] (58) 
 Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)
 Erythema [MESH:D004890] (1330) 
 Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)
 Facial Dermatoses [MESH:D005148] (1336) 
 Acneiform Eruptions [MESH:D017486] (1312) 
 Chloracne [MESH:D054506] (1274)
 Hair Diseases [MESH:D006201] (1891) 
 Pseudofolliculitis Barbae [MESH:C563016] (16)
 Hypotrichosis [MESH:D007039] (1513) 
 Alopecia [MESH:D000505] (1453) 
 Dermatopathia pigmentosa reticularis [MESH:C535374] (38)
 Keratosis [MESH:D007642] (1941) 
 Ichthyosis [MESH:D007057] (481) 
 Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)
 Ichthyosis Vulgaris [MESH:D016112] (27)
 Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238) 
 Hyperkeratosis, Epidermolytic [MESH:D017488] (136) 
 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)
 Ichthyosis, Lamellar [MESH:D017490] (81) 
 Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)
 Keratoderma, Palmoplantar [MESH:D007645] (287) 
 Keratosis palmoplantaris striata 1 [MESH:C536162] (54)
 Keratosis palmoplantaris striata 3 [MESH:C536163] (48)
 Naegeli syndrome [MESH:C538331] (38)
 Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80) 
 Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)
 Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)
 Nail Diseases [MESH:D009260] (203) 
 Dermatopathia pigmentosa reticularis [MESH:C535374] (38)
 Pachyonychia Congenita [MESH:D053549] (80) 
 Steatocystoma Multiplex [MESH:D062685] (56)
 Pigmentation Disorders [MESH:D010859] (1215) 
 Hyperpigmentation [MESH:D017495] (523) 
 Dermatopathia pigmentosa reticularis [MESH:C535374] (38)
 dowling-degos disease [MESH:C562924] (53)
 Sebaceous Gland Diseases [MESH:D012625] (245) 
 Dermatitis, Seborrheic [MESH:D012628] (58) 
 Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)
 Skin Abnormalities [MESH:D012868] (1709) 
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Naegeli syndrome [MESH:C538331] (38)
 Pachyonychia Congenita [MESH:D053549] (80) 
 Steatocystoma Multiplex [MESH:D062685] (56)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Epidermolysis Bullosa Simplex [MESH:D016110] (140) 
 Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)
 Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)
 Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)
 Ichthyosis [MESH:D007057] (481) 
 Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)
 Ichthyosis Vulgaris [MESH:D016112] (27)
 Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238) 
 Hyperkeratosis, Epidermolytic [MESH:D017488] (136) 
 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)
 Ichthyosis, Lamellar [MESH:D017490] (81) 
 Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)
 Skin Diseases, Eczematous [MESH:D017443] (3740) 
 Eczema [MESH:D004485] (235)
 Dermatitis, Atopic [MESH:D003876] (2052) 
 Dermatitis, Atopic, 2 [MESH:C565293] (26)
 Dermatitis, Atopic, 1 [MESH:C566404] (26)
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 Dermatitis, Seborrheic [MESH:D012628] (58) 
 Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)
 Skin Diseases, Genetic [MESH:D012873] (3481) 
 dowling-degos disease [MESH:C562924] (53)
 Ichthyosis Vulgaris [MESH:D016112] (27)
 Dermatitis, Atopic [MESH:D003876] (2052) 
 Dermatitis, Atopic, 2 [MESH:C565293] (26)
 Dermatitis, Atopic, 1 [MESH:C566404] (26)
 Ectodermal Dysplasia [MESH:D004476] (958) 
 Naegeli syndrome [MESH:C538331] (38)
 Pachyonychia Congenita [MESH:D053549] (80) 
 Steatocystoma Multiplex [MESH:D062685] (56)
 Ehlers-Danlos Syndrome [MESH:D004535] (491) 
 Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)
 Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Epidermolysis Bullosa Simplex [MESH:D016110] (140) 
 Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)
 Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)
 Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)
 Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238) 
 Hyperkeratosis, Epidermolytic [MESH:D017488] (136) 
 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)
 Ichthyosis, Lamellar [MESH:D017490] (81) 
 Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)
 Keratoderma, Palmoplantar [MESH:D007645] (287) 
 Keratosis palmoplantaris striata 1 [MESH:C536162] (54)
 Keratosis palmoplantaris striata 3 [MESH:C536163] (48)
 Naegeli syndrome [MESH:C538331] (38)
 Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80) 
 Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)
 Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)
 Skin Diseases, Infectious [MESH:D012874] (2684) 
 Skin Diseases, Parasitic [MESH:D012876] (2526) 
 Leishmaniasis [MESH:D007896] (2516) 
 Leishmaniasis, Cutaneous [MESH:D016773] (2359)
 Skin Diseases, Papulosquamous [MESH:D017444] (3392) 
 dowling-degos disease [MESH:C562924] (53)
 Psoriasis [MESH:D011565] (3278)
 Dermatitis, Seborrheic [MESH:D012628] (58) 
 Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)
 Skin Diseases, Vascular [MESH:D017445] (3288) 
 Behcet Syndrome [MESH:D001528] (1784)
 Urticaria [MESH:D014581] (2668) 
 Angioedema [MESH:D000799] (837)
 Skin Diseases, Vesiculobullous [MESH:D012872] (1754) 
 Epidermolysis Bullosa [MESH:D004820] (260) 
 Epidermolysis Bullosa, Junctional [MESH:D016109] (152) 
 Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)
 Epidermolysis Bullosa Simplex [MESH:D016110] (140) 
 Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)
 Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)
 Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)
 Skin Neoplasms [MESH:D012878] (2991) 
 Dermatopathia pigmentosa reticularis [MESH:C535374] (38)
 Sweat Gland Diseases [MESH:D013543] (231) 
 Hypohidrosis [MESH:D007007] (47) 
 Naegeli syndrome [MESH:C538331] (38)
C18. Nutritional and Metabolic Diseases 
C18. Nutritional and Metabolic Diseases
 Metabolic Diseases [MESH:D008659] (9025) 
 Brain Diseases, Metabolic [MESH:D001928] (3350) 
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Calcium Metabolism Disorders [MESH:D002128] (3634) 
 Calcinosis [MESH:D002114] (2989)
 Glucose Metabolism Disorders [MESH:D044882] (6122) 
 Hyperglycemia [MESH:D006943] (1858)
 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)
 Hyperinsulinism [MESH:D006946] (3586) 
 Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)
 Hypoglycemia [MESH:D007003] (2420) 
 Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)
 Lipid Metabolism Disorders [MESH:D052439] (3225) 
 Lipidoses [MESH:D008064] (1655) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Xanthomatosis [MESH:D014973] (145) 
 Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)
 Malabsorption Syndromes [MESH:D008286] (1869) 
 Celiac Disease [MESH:D002446] (340)
 Metabolism, Inborn Errors [MESH:D008661] (6028) 
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559) 
 Glutamine deficiency, congenital [MESH:C536832] (117)
 Methylmalonic acidemia [MESH:C537358] (764)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 MELAS Syndrome [MESH:D017241] (1061)
 MERRF Syndrome [MESH:D017243] (1053)
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100) 
 Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (195)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)
 Lipidoses [MESH:D008064] (1655) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Lysosomal Storage Diseases [MESH:D016464] (761) 
 Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636) 
 Sphingolipidoses [MESH:D013106] (582) 
 Gaucher Disease [MESH:D005776] (299) 
 Gaucher-like disease [MESH:C537675] (17)
 Gaucher Disease, Perinatal Lethal [MESH:C564306] (17)
 Peroxisomal Disorders [MESH:D018901] (1788) 
 Acatalasia [MESH:D020642] (788)
 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)
 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)
 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) 
 Adrenal Gland Diseases [MESH:D000307] (2397) 
 Adrenal Cortex Diseases [MESH:D000303] (969) 
 Adrenal Cortex Neoplasms [MESH:D000306] (823) 
 Adrenocortical Carcinoma [MESH:D018268] (821)
 Adrenal Gland Neoplasms [MESH:D000310] (917) 
 Adrenal Cortex Neoplasms [MESH:D000306] (823) 
 Adrenocortical Carcinoma [MESH:D018268] (821)
 Diabetes Mellitus [MESH:D003920] (6159) 
 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 Neuropathies [MESH:D003929] (2443)
 Diabetic Angiopathies [MESH:D003925] (1984) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Ovarian Neoplasms [MESH:D010051] (3275)
 Pancreatic Neoplasms [MESH:D010190] (3820)
 Thyroid Neoplasms [MESH:D013964] (2040)
 Adrenal Gland Neoplasms [MESH:D000310] (917) 
 Adrenal Cortex Neoplasms [MESH:D000306] (823) 
 Adrenocortical Carcinoma [MESH:D018268] (821)
 Pituitary Neoplasms [MESH:D010911] (981) 
 ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Prolactinoma [MESH:D015175] (312)
 Gonadal Disorders [MESH:D006058] (5088) 
 Puberty, Precocious [MESH:D011629] (1147)
 Ovarian Diseases [MESH:D010049] (4253) 
 Ovarian Cysts [MESH:D010048] (2534)
 Ovarian Neoplasms [MESH:D010051] (3281)
 Pituitary Diseases [MESH:D010900] (1829) 
 Hyperpituitarism [MESH:D006964] (1259) 
 Acromegaly [MESH:D000172] (466)
 Pituitary Neoplasms [MESH:D010911] (981) 
 ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)
 Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)
 Prolactinoma [MESH:D015175] (312)
 Thyroid Diseases [MESH:D013959] (2808) 
 Thyroid Neoplasms [MESH:D013964] (2040)
C20. Immune System Diseases 
C20. Immune System Diseases
 Immune System Diseases [MESH:D007154] (7674) 
 Autoimmune Diseases [MESH:D001327] (5067) 
 Arthritis, Rheumatoid [MESH:D001172] (3601)
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1893)
 Hepatitis, Autoimmune [MESH:D019693] (1982)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Myasthenia Gravis [MESH:D009157] (632)
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Hypersensitivity [MESH:D006967] (5873) 
 Drug Hypersensitivity [MESH:D004342] (4000) 
 Asthma, Aspirin-Induced [MESH:D055963] (1055)
 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) 
 Dermatitis, Atopic, 2 [MESH:C565293] (26)
 Dermatitis, Atopic, 1 [MESH:C566404] (26)
 Respiratory Hypersensitivity [MESH:D012130] (4250) 
 Asthma [MESH:D001249] (3914)
 Urticaria [MESH:D014581] (2668) 
 Angioedema [MESH:D000799] (837)
 Immunologic Deficiency Syndromes [MESH:D007153] (3788) 
 Lymphopenia [MESH:D008231] (990)
 HIV Infections [MESH:D015658] (3402) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Phagocyte Bactericidal Dysfunction [MESH:D010585] (999) 
 Granulomatous Disease, Chronic [MESH:D006105] (404)
 Immunoproliferative Disorders [MESH:D007160] (4761) 
 Lymphoproliferative Disorders [MESH:D008232] (4734) 
 Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)
 Multiple Myeloma [MESH:D009101] (2767)
 Leukemia, Lymphoid [MESH:D007945] (3047) 
 Leukemia, B-Cell [MESH:D015448] (2564) 
 Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
 Lymphoma [MESH:D008223] (3684) 
 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, T-Cell, Cutaneous [MESH:D016410] (912)
 Paraproteinemias [MESH:D010265] (2791) 
 Multiple Myeloma [MESH:D009101] (2765)
C22. Animal Diseases 
C22. Animal Diseases
 Animal Diseases [MESH:D000820] (3656) 
 Disease Models, Animal [MESH:D004195] (2058)
 Hepatitis, Animal [MESH:D006520] (260)
 Mammary Neoplasms, Animal [MESH:D015674] (2735)
C23. Pathological Conditions, Signs and Symptoms 
C23. Pathological Conditions, Signs and Symptoms
 Pathological Conditions, Anatomical [MESH:D020763] (6074) 
 Alopecia [MESH:D000505] (1383) 
 Dermatopathia pigmentosa reticularis [MESH:C535374] (38)
 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) 
 Arrhythmias, Cardiac [MESH:D001145] (4658)
 Gliosis [MESH:D005911] (1419)
 Hemolysis [MESH:D006461] (280)
 Hyperplasia [MESH:D006965] (2463)
 Leukocytosis [MESH:D007964] (978)
 Necrosis [MESH:D009336] (4019)
 Nerve Degeneration [MESH:D009410] (4061)
 Chromosome Aberrations [MESH:D002869] (2352) 
 Micronuclei, Chromosome-Defective [MESH:D048629] (1013)
 Disease Attributes [MESH:D020969] (3654) 
 Disease Progression [MESH:D018450] (2868)
 Disease Susceptibility [MESH:D004198] (1200)
 Recurrence [MESH:D012008] (830)
 Fibrosis [MESH:D005355] (3133) 
 Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)
 Cicatrix [MESH:D002921] (1115) 
 Keloid [MESH:D007627] (1110)
 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)
 Hematoma [MESH:D006406] (281) 
 Hematoma, Epidural, Spinal [MESH:D046748] (167)
 Hematoma, Subdural [MESH:D006408] (215)
 Intracranial Hemorrhages [MESH:D020300] (3241) 
 Cerebral Hemorrhage [MESH:D002543] (2872)
 Hematoma, Subdural [MESH:D006408] (212)
 Inflammation [MESH:D007249] (5241) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Systemic Inflammatory Response Syndrome [MESH:D018746] (3563) 
 Sepsis [MESH:D018805] (3562) 
 Bacteremia [MESH:D016470] (1369)
 Neoplastic Processes [MESH:D009385] (5317) 
 Neoplasm Invasiveness [MESH:D009361] (3388)
 Neoplasm Recurrence, Local [MESH:D009364] (1949)
 Carcinogenesis [MESH:D063646] (3391) 
 Cell Transformation, Neoplastic [MESH:D002471] (3389)
 Neoplasm Metastasis [MESH:D009362] (4441) 
 Lymphatic Metastasis [MESH:D008207] (917)
 Ossification, Heterotopic [MESH:D009999] (187) 
 Ossification of Posterior Longitudinal Ligament [MESH:D017887] (99) 
 Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98)
 Postoperative Complications [MESH:D011183] (5311) 
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Sclerosis [MESH:D012598] (224) 
 Scleroatonic muscular dystrophy [MESH:C537521] (108)
 Shock [MESH:D012769] (2550) 
 Shock, Cardiogenic [MESH:D012770] (269)
 Shock, Hemorrhagic [MESH:D012771] (2042)
 Signs and Symptoms [MESH:D012816] (10659) 
 Edema [MESH:D004487] (3726)
 Flushing [MESH:D005483] (506)
 Body Temperature Changes [MESH:D001832] (3130) 
 Fever [MESH:D005334] (2856)
 Body Weight [MESH:D001835] (4972) 
 Body Weight Changes [MESH:D001836] (3206) 
 Weight Gain [MESH:D015430] (2595)
 Weight Loss [MESH:D015431] (2512) 
 Emaciation [MESH:D004614] (2285) 
 Cachexia [MESH:D002100] (2283)
 Overweight [MESH:D050177] (4455) 
 Obesity [MESH:D009765] (4454)
 Neurologic Manifestations [MESH:D009461] (8702) 
 Paresis [MESH:D010291] (419)
 Seizures [MESH:D012640] (4502)
 Dyskinesias [MESH:D020820] (3285) 
 Hypokinesia [MESH:D018476] (279)
 Neurobehavioral Manifestations [MESH:D019954] (4706) 
 Lethargy [MESH:D053609] (1035)
 Memory Disorders [MESH:D008569] (3233)
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Language Disorders [MESH:D007806] (653) 
 Speech Disorders [MESH:D013064] (482) 
 Aphasia [MESH:D001037] (219)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Muscular Atrophy [MESH:D009133] (1234)
 Pain [MESH:D010146] (3869) 
 Back Pain [MESH:D001416] (285) 
 Low Back Pain [MESH:D017116] (244)
 Paralysis [MESH:D010243] (2298) 
 Ophthalmoplegia [MESH:D009886] (1468) 
 Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)
 Sensation Disorders [MESH:D012678] (5009) 
 Taste Disorders [MESH:D013651] (461)
 Hearing Disorders [MESH:D006311] (2101) 
 Hearing Loss [MESH:D034381] (2066) 
 Hearing Loss, Sensorineural [MESH:D006319] (1227) 
 Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)
 Somatosensory Disorders [MESH:D020886] (4000) 
 Hyperalgesia [MESH:D006930] (3929)
 Sleep Disorders [MESH:D012893] (1301) 
 Sleep Deprivation [MESH:D012892] (233)
 Pain [MESH:D010146] (4511) 
 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)
 Urological Manifestations [MESH:D020924] (3532) 
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
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)
 Poisoning [MESH:D011041] (6703) 
 Arsenic Poisoning [MESH:D020261] (2540)
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Manganese Poisoning [MESH:D020149] (2214)
 Foodborne Diseases [MESH:D005517] (269) 
 Favism [MESH:D005236] (193)
 Neurotoxicity Syndromes [MESH:D020258] (3323) 
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Plant Poisoning [MESH:D010939] (208) 
 Favism [MESH:D005236] (193)
 Substance-Related Disorders [MESH:D019966] (6308) 
 Amphetamine-Related Disorders [MESH:D019969] (2858)
 Alcohol-Related Disorders [MESH:D019973] (3869) 
 Alcohol-Induced Disorders [MESH:D020751] (3350) 
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
C26. Wounds and Injuries 
C26. Wounds and Injuries
 Z. Exceptions (2454) 
 Not Fully Specified [NFS] (2454)
 Wounds and Injuries [MESH:D014947] (5171) 
 Burns [MESH:D002056] (2565)
 Craniocerebral Trauma [MESH:D006259] (3523) 
 Brain Injuries [MESH:D001930] (3431)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (217) 
 Hematoma, Subdural [MESH:D006408] (212)
 Radiation Injuries [MESH:D011832] (2718) 
 Radiation Injuries, Experimental [MESH:D011833] (2662)
 Spinal Cord Injuries [MESH:D013119] (2688) 
 Spinal Cord Compression [MESH:D013117] (1800)
 Trauma, Nervous System [MESH:D020196] (3535) 
 Craniocerebral Trauma [MESH:D006259] (3507) 
 Brain Injuries [MESH:D001930] (3431)
 Intracranial Hemorrhage, Traumatic [MESH:D020198] (221) 
 Hematoma, Subdural [MESH:D006408] (212)
D02. Organic Chemicals 
D02. Organic Chemicals
 Organic Chemicals [MESH:D009930] (75987) 
 Hydrocarbons [MESH:D006838] (35762) 
 Hydrocarbons, Acyclic [MESH:D006839] (3563) 
 Alkenes [MESH:D000475] (2079) 
 Polyenes [MESH:D011090] (1230) 
 Carotenoids [MESH:D002338] (585) 
 Retinoids [MESH:D012176] (281) 
 Vitamin A [MESH:D014801] (141) 
 Tretinoin [MESH:D014212] (83)
 Hydrocarbons, Cyclic [MESH:D006844] (22983) 
 Hydrocarbons, Alicyclic [MESH:D006840] (3199) 
 Cycloparaffins [MESH:D003516] (3197) 
 Cyclohexanes [MESH:D003510] (1589) 
 Cyclohexenes [MESH:D053138] (756) 
 Carotenoids [MESH:D002338] (579) 
 Retinoids [MESH:D012176] (275) 
 Vitamin A [MESH:D014801] (141) 
 Tretinoin [MESH:D014212] (83)
 Terpenes [MESH:D013729] (10347) 
 Carotenoids [MESH:D002338] (585) 
 Retinoids [MESH:D012176] (281) 
 Vitamin A [MESH:D014801] (141) 
 Tretinoin [MESH:D014212] (83)
D23. Biological Factors 
D23. Biological Factors
 Biological Factors [MESH:D001685] (12003) 
 Pigments, Biological [MESH:D010860] (2018) 
 Carotenoids [MESH:D002338] (508) 
 Retinoids [MESH:D012176] (281) 
 Tretinoin [MESH:D014212] (83)