more general categories |
information about this item |
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1. Human Genes |
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1. Human Genes |
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cadherin 1, type 1, E-cadherin (epithelial) [HGNC:CDH1] (122) |
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desmocollin 1 [HGNC:DSC1] (12) |
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S100 calcium binding protein A01 [HGNC:S100A1] (10) |
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S100 calcium binding protein A07 [HGNC:S100A7] (9) |
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S100 calcium binding protein A08 [HGNC:S100A8] (31) |
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S100 calcium binding protein A09 [HGNC:S100A9] (33) |
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cadherin 01, type 1, E-cadherin (epithelial) [HGNC:CDH1] (122) |
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integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor) [HGNC:ITGA4] (22) |
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interleukin 10 receptor, alpha [HGNC:IL10RA] (14) |
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collagen, type I, alpha 1 [HGNC:COL1A1] (123) |
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collagen, type IV, alpha 2 [HGNC:COL4A2] (26) |
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collagen, type VI, alpha 1 [HGNC:COL6A1] (28) |
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collagen, type VIII, alpha 2 [HGNC:COL8A2] (11) |
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oxidized low density lipoprotein (lectin-like) receptor 1 [HGNC:OLR1] (40) |
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cytochrome P450, family 26, subfamily A, polypeptide 01 [HGNC:CYP26A1] (32) |
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cytochrome P450, family 27, subfamily A, polypeptide 01 [HGNC:CYP27A1] (34) |
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filaggrin [HGNC:FLG] (11) |
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S100 calcium binding protein A01 [HGNC:S100A1] (10) |
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S100 calcium binding protein A07 [HGNC:S100A7] (9) |
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S100 calcium binding protein A08 [HGNC:S100A8] (31) |
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S100 calcium binding protein A09 [HGNC:S100A9] (33) |
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chemokine (C-X-C motif) ligand 01 (melanoma growth stimulating activity, alpha) [HGNC:CXCL1] (82) |
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cellular retinoic acid binding protein 2 [HGNC:CRABP2] (32) |
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fatty acid binding protein 5 (psoriasis-associated) [HGNC:FABP5] (29) |
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forkhead box A1 [HGNC:FOXA1] (30) |
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GATA binding protein 6 [HGNC:GATA6] (38) |
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glutathione S-transferase mu 1 [HGNC:GSTM1] (144) |
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mesenchyme homeobox 1 [HGNC:MEOX1] (14) |
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Meis homeobox 1 [HGNC:MEIS1] (13) |
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integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor) [HGNC:ITGA4] (22) |
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interleukin 01, beta [HGNC:IL1B] (497) |
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interleukin 10 receptor, alpha [HGNC:IL10RA] (14) |
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interleukin 24 [HGNC:IL24] (37) |
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keratin 10 [HGNC:KRT10] (27) |
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keratin 14 [HGNC:KRT14] (13) |
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keratin 15 [HGNC:KRT15] (23) |
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keratin 17 [HGNC:KRT17] (36) |
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keratin 18 [HGNC:KRT18] (50) |
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keratin 19 [HGNC:KRT19] (40) |
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keratin 01 [HGNC:KRT1] (24) |
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keratin 05 [HGNC:KRT5] (25) |
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keratin 06A [HGNC:KRT6A] (18) |
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keratin 07 [HGNC:KRT7] (30) |
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keratin 08 [HGNC:KRT8] (53) |
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keratin 75 [HGNC:KRT75] (10) |
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neurofilament, light polypeptide [HGNC:NEFL] (22) |
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keratin 01 [HGNC:KRT1] (24) |
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keratin 05 [HGNC:KRT5] (25) |
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keratin 06A [HGNC:KRT6A] (18) |
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keratin 07 [HGNC:KRT7] (30) |
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keratin 08 [HGNC:KRT8] (53) |
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keratin 10 [HGNC:KRT10] (27) |
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keratin 14 [HGNC:KRT14] (13) |
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keratin 15 [HGNC:KRT15] (23) |
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keratin 17 [HGNC:KRT17] (36) |
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keratin 18 [HGNC:KRT18] (50) |
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keratin 19 [HGNC:KRT19] (40) |
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keratin 75 [HGNC:KRT75] (10) |
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laminin, alpha 2 [HGNC:LAMA2] (11) |
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laminin, alpha 3 [HGNC:LAMA3] (25) |
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laminin, gamma 3 [HGNC:LAMC3] (6) |
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lipocalin 2 [HGNC:LCN2] (25) |
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retinoic acid receptor, alpha [HGNC:RARA] (73) |
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retinoic acid receptor, beta [HGNC:RARB] (56) |
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growth factor receptor-bound protein 07 [HGNC:GRB7] (16) |
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dual specificity phosphatase 10 [HGNC:DUSP10] (34) |
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serpin peptidase inhibitor, clade B (ovalbumin), member 02 [HGNC:SERPINB2] (63) |
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serpin peptidase inhibitor, clade B (ovalbumin), member 09 [HGNC:SERPINB9] (27) |
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growth factor receptor-bound protein 07 [HGNC:GRB7] (16) |
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suppressor of cytokine signaling 1 [HGNC:SOCS1] (25) |
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suppressor of cytokine signaling 2 [HGNC:SOCS2] (31) |
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fatty acid synthase [HGNC:FASN] (72) |
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solute carrier family 16 (monocarboxylate transporter), member 1 [HGNC:SLC16A1] (43) |
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sulfotransferase family, cytosolic, 2A, dehydroepiandrosterone (DHEA)-preferring, member 1 [HGNC:SULT2A1] (47) |
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suppressor of cytokine signaling 1 [HGNC:SOCS1] (25) |
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suppressor of cytokine signaling 2 [HGNC:SOCS2] (31) |
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transglutaminase 1 [HGNC:TGM1] (15) |
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transglutaminase 2 [HGNC:TGM2] (60) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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expression (494) |
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expression (2187) |
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chemical synthesis (464) |
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expression (3238) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Bacteremia [MESH:D016470] (208) |
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Helicobacter Infections [MESH:D016481] (579) |
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Mycoplasma Infections [MESH:D009175] (1947) |
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Bacteremia [MESH:D016470] (1369) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Entamoebiasis [MESH:D004749] (1689) |
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Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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Malaria, Falciparum [MESH:D016778] (438) |
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Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
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C04. Neoplasms |
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C04. Neoplasms |
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Neoplasms, Second Primary [MESH:D016609] (518) |
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Ovarian Cysts [MESH:D010048] (2534) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
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Wilms Tumor [MESH:D009396] (553) |
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Liposarcoma [MESH:D008080] (612) |
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Osteosarcoma [MESH:D012516] (2175) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Rhabdomyosarcoma [MESH:D012208] (789) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Liposarcoma [MESH:D008080] (612) |
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Osteosarcoma [MESH:D012516] (2175) |
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Rhabdomyosarcoma [MESH:D012208] (789) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (169) |
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Adenoma, Oxyphilic [MESH:D018249] (115) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Mesothelioma [MESH:D008654] (2567) |
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Prolactinoma [MESH:D015175] (312) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Basal Cell [MESH:D002280] (1628) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adrenocortical Carcinoma [MESH:D018268] (821) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Lobular [MESH:D018275] (305) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Cholangiocarcinoma [MESH:D018281] (2398) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Basal Cell [MESH:D002280] (1628) |
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Carcinoma, Lobular [MESH:D018275] (305) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Mesothelioma [MESH:D008654] (2567) |
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Glioblastoma [MESH:D005909] (2554) |
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Papilloma [MESH:D010212] (2243) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Melanoma [MESH:D008545] (3508) |
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Bone Neoplasms [MESH:D001859] (1334) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Bile Duct Neoplasms [MESH:D001650] (367) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Adrenocortical Carcinoma [MESH:D018268] (821) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Prolactinoma [MESH:D015175] (312) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Pituitary Neoplasms [MESH:D010911] (914) |
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Dermatopathia pigmentosa reticularis [MESH:C535374] (38) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Small Cell Lung Carcinoma [MESH:D055752] (1380) |
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Endometrial Neoplasms [MESH:D016889] (1987) |
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Uterine Cervical Neoplasms [MESH:D002583] (978) |
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Prostate cancer, familial [MESH:C537243] (264) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Wilms Tumor [MESH:D009396] (553) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Lymphatic Metastasis [MESH:D008207] (917) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Wilms Tumor [MESH:D009396] (553) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Bone Neoplasms [MESH:D001859] (1334) |
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Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
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Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
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Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
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Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
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Acromegaly [MESH:D000172] (466) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
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Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Osteoarthritis [MESH:D010003] (1743) |
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Bethlem myopathy [MESH:C535436] (108) |
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Erythrocyte Lactate Transporter Defect [MESH:C565449] (106) |
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Bethlem myopathy [MESH:C535436] (108) |
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MELAS Syndrome [MESH:D017241] (1061) |
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MERRF Syndrome [MESH:D017243] (1053) |
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Kearns-Sayre Syndrome [MESH:D007625] (1054) |
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Bethlem myopathy [MESH:C535436] (108) |
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Muscular dystrophy congenital, merosin negative [MESH:C537384] (34) |
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Scleroatonic muscular dystrophy [MESH:C537521] (108) |
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Dermatomyositis [MESH:D003882] (1826) |
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Dermatomyositis [MESH:D003882] (1826) |
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Silver-Russell Syndrome [MESH:D056730] (142) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Osteoarthritis [MESH:D010003] (1743) |
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C06. Digestive System Diseases |
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C06. Digestive System Diseases |
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Bile Duct Neoplasms [MESH:D001650] (367) |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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Bile Duct Neoplasms [MESH:D001650] (367) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Bile Duct Neoplasms [MESH:D001650] (367) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Gastroesophageal Reflux [MESH:D005764] (1465) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Mucositis [MESH:D052016] (1238) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Enterocolitis, Necrotizing [MESH:D020345] (1367) |
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Gastritis, Atrophic [MESH:D005757] (947) |
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Inflammatory Bowel Disease 28, Autosomal Recessive [MESH:C567728] (43) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Enterocolitis, Necrotizing [MESH:D020345] (1367) |
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Inflammatory Bowel Disease 28, Autosomal Recessive [MESH:C567728] (43) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Celiac Disease [MESH:D002446] (340) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Gastritis, Atrophic [MESH:D005757] (947) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
|
|
|
|
|
Liver Failure, Acute [MESH:D017114] (2404) |
|
|
Hepatitis, Animal [MESH:D006520] (260) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Cirrhosis, Familial [MESH:C566123] (179) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
Pancreatic Neoplasms [MESH:D010190] (3820) |
|
|
Pancreatitis [MESH:D010195] (1924) |
|
 |
C07. Stomatognathic Diseases |
 |
 |
|
C07. Stomatognathic Diseases |
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Mucositis [MESH:D052016] (1238) |
|
|
Oral Submucous Fibrosis [MESH:D009914] (2432) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
Tongue Neoplasms [MESH:D014062] (1518) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
Tongue Neoplasms [MESH:D014062] (1518) |
|
|
|
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
 |
C08. Respiratory Tract Diseases |
 |
 |
|
C08. Respiratory Tract Diseases |
|
|
|
|
|
Bronchial Hyperreactivity [MESH:D016535] (1357) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Laryngo onycho cutaneous syndrome [MESH:C537032] (49) |
|
|
Hypertension, Pulmonary [MESH:D006976] (2000) |
|
|
Pneumonia [MESH:D011014] (3482) |
|
|
Pulmonary Edema [MESH:D011654] (2109) |
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Pulmonary Fibrosis [MESH:D011658] (3140) |
|
|
|
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Asthma [MESH:D001249] (3903) |
|
|
Acute Lung Injury [MESH:D055371] (1907) |
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
|
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Pneumonia [MESH:D011014] (3482) |
|
|
|
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
 |
C09. Otorhinolaryngologic Diseases |
 |
 |
|
C09. Otorhinolaryngologic Diseases |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
|
|
Laryngo onycho cutaneous syndrome [MESH:C537032] (49) |
|
|
|
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
|
|
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
|
Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
|
 |
C10. Nervous System Diseases |
 |
 |
|
C10. Nervous System Diseases |
|
|
Not Fully Specified [NFS] (4027) |
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
Myasthenia Gravis [MESH:D009157] (632) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
|
|
|
Lewy Body Disease [MESH:D020961] (1143) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
Vasospasm, Intracranial [MESH:D020301] (324) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Intracranial Thrombosis [MESH:D020767] (481) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Hematoma, Subdural [MESH:D006408] (212) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
Lewy Body Disease [MESH:D020961] (1143) |
|
|
Meningoencephalitis [MESH:D008590] (179) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
|
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Epilepsy, Tonic-Clonic [MESH:D004830] (1042) |
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
|
|
|
Acromegaly [MESH:D000172] (466) |
|
|
ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172) |
|
|
Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
|
|
Prolactinoma [MESH:D015175] (312) |
|
|
Meningoencephalitis [MESH:D008590] (207) |
|
|
Meningoencephalitis [MESH:D008590] (179) |
|
|
Meningoencephalitis [MESH:D008590] (179) |
|
|
Meningoencephalitis [MESH:D008590] (179) |
|
|
|
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Lewy Body Disease [MESH:D020961] (1143) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Spinal Cord Compression [MESH:D013117] (1800) |
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
|
|
Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
Lewy Body Disease [MESH:D020961] (1143) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
|
|
Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Paresis [MESH:D010291] (419) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Hypokinesia [MESH:D018476] (279) |
|
|
Lethargy [MESH:D053609] (1035) |
|
|
Memory Disorders [MESH:D008569] (3233) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
|
|
|
Aphasia [MESH:D001037] (219) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
|
|
|
Low Back Pain [MESH:D017116] (244) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
Taste Disorders [MESH:D013651] (461) |
|
|
|
|
|
|
|
|
Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Erythrocyte Lactate Transporter Defect [MESH:C565449] (106) |
|
|
|
|
|
Bethlem myopathy [MESH:C535436] (108) |
|
|
Muscular dystrophy congenital, merosin negative [MESH:C537384] (34) |
|
|
Scleroatonic muscular dystrophy [MESH:C537521] (108) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Myasthenia Gravis [MESH:D009157] (632) |
|
|
Diabetic Neuropathies [MESH:D003929] (2442) |
|
|
Sciatic Neuropathy [MESH:D020426] (477) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
|
|
Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
Sleep Deprivation [MESH:D012892] (233) |
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
Narcolepsy [MESH:D009290] (478) |
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
|
Hematoma, Subdural [MESH:D006408] (212) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
|
|
|
Laryngo onycho cutaneous syndrome [MESH:C537032] (49) |
|
|
|
|
|
Corneal Dystrophy, Posterior Polymorphous, 1 [MESH:C562745] (25) |
|
|
Corneal Dystrophy, Posterior Polymorphous, 2 [MESH:C565176] (18) |
|
|
Corneal dystrophy, Fuchs' endothelial, 1 [MESH:C535478] (18) |
|
|
|
|
|
Corneal Dystrophy, Posterior Polymorphous, 1 [MESH:C562745] (25) |
|
|
Corneal Dystrophy, Posterior Polymorphous, 2 [MESH:C565176] (18) |
|
|
Corneal dystrophy, Fuchs' endothelial, 1 [MESH:C535478] (18) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Dry Eye Syndromes [MESH:D015352] (533) |
|
|
|
|
|
Glaucoma, Open-Angle [MESH:D005902] (1281) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Myopia [MESH:D009216] (349) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
|
|
|
|
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
|
|
|
Prostate cancer, familial [MESH:C537243] (264) |
|
|
|
|
|
Prostate cancer, familial [MESH:C537243] (264) |
|
|
|
|
|
|
|
|
Prostate cancer, familial [MESH:C537243] (264) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Wilms Tumor [MESH:D009396] (553) |
|
|
|
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
|
|
|
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Wilms Tumor [MESH:D009396] (553) |
|
|
Glomerulonephritis [MESH:D005921] (3758) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
 |
C13. Female Urogenital Diseases and Pregnancy Complications |
 |
 |
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
Not Fully Specified [NFS] (1116) |
|
|
|
|
|
Endometriosis [MESH:D004715] (2461) |
|
|
|
|
|
Ovarian Cysts [MESH:D010048] (2534) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Endometrial Hyperplasia [MESH:D004714] (263) |
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Wilms Tumor [MESH:D009396] (553) |
|
|
|
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
|
|
|
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Wilms Tumor [MESH:D009396] (553) |
|
|
Glomerulonephritis [MESH:D005921] (3758) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Placenta Diseases [MESH:D010922] (1781) |
|
|
Polyhydramnios [MESH:D006831] (123) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Arrhythmias, Cardiac [MESH:D001145] (4679) |
|
|
Cardiac Tamponade [MESH:D002305] (175) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Pericardial Effusion [MESH:D010490] (1015) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Aortic Valve Insufficiency [MESH:D001022] (1002) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Thrombosis [MESH:D003328] (255) |
|
|
Shock, Cardiogenic [MESH:D012770] (269) |
|
|
Ventricular Dysfunction, Left [MESH:D018487] (1631) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypertension [MESH:D006973] (5655) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Aneurysm, Dissecting [MESH:D000784] (699) |
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
|
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Vasospasm, Intracranial [MESH:D020301] (324) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Intracranial Thrombosis [MESH:D020767] (481) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Hematoma, Subdural [MESH:D006408] (212) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
|
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Embolism, Cholesterol [MESH:D017700] (255) |
|
|
Venous Thromboembolism [MESH:D054556] (400) |
|
|
Intracranial Thrombosis [MESH:D020767] (481) |
|
|
Coronary Thrombosis [MESH:D003328] (255) |
|
|
Venous Thrombosis [MESH:D020246] (1141) |
|
|
Venous Thromboembolism [MESH:D054556] (400) |
|
|
Intracranial Thrombosis [MESH:D020767] (481) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Thrombosis [MESH:D003328] (255) |
|
|
Shock, Cardiogenic [MESH:D012770] (269) |
|
|
Raynaud Disease [MESH:D011928] (490) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
Not Fully Specified [NFS] (453) |
|
|
|
|
|
Anemia, Sideroblastic [MESH:D000756] (636) |
|
|
Favism [MESH:D005236] (193) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308) |
|
|
Favism [MESH:D005236] (193) |
|
|
beta-Thalassemia [MESH:D017086] (458) |
|
|
|
|
|
|
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
Anemia, Sideroblastic [MESH:D000756] (636) |
|
|
|
|
|
beta-Thalassemia [MESH:D017086] (458) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
Leukocytosis [MESH:D007964] (988) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
Granulomatous Disease, Chronic [MESH:D006105] (404) |
|
|
|
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
|
|
|
|
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
|
Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
|
|
Hypersplenism [MESH:D006971] (341) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
Abnormalities, Drug-Induced [MESH:D000014] (1024) |
|
|
Beckwith-Wiedemann Syndrome [MESH:D001506] (193) |
|
|
Silver-Russell Syndrome [MESH:D056730] (142) |
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
|
Beckwith-Wiedemann Syndrome [MESH:D001506] (193) |
|
|
Silver-Russell Syndrome [MESH:D056730] (142) |
|
|
Craniofacial Abnormalities [MESH:D019465] (3064) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
|
|
Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
|
|
|
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
|
Steatocystoma Multiplex [MESH:D062685] (56) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
|
|
|
Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150) |
|
|
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 hystrix, Curth Macklin type [MESH:C536088] (48) |
|
|
Ichthyosis Vulgaris [MESH:D016112] (27) |
|
|
|
|
|
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84) |
|
|
Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
Cirrhosis, Familial [MESH:C566123] (179) |
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
|
|
Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308) |
|
|
Favism [MESH:D005236] (193) |
|
|
beta-Thalassemia [MESH:D017086] (458) |
|
|
Beckwith-Wiedemann Syndrome [MESH:D001506] (193) |
|
|
Silver-Russell Syndrome [MESH:D056730] (142) |
|
|
Silver-Russell Syndrome [MESH:D056730] (142) |
|
|
|
|
|
Corneal Dystrophy, Posterior Polymorphous, 1 [MESH:C562745] (25) |
|
|
Corneal Dystrophy, Posterior Polymorphous, 2 [MESH:C565176] (18) |
|
|
Corneal dystrophy, Fuchs' endothelial, 1 [MESH:C535478] (18) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Granulomatous Disease, Chronic [MESH:D006105] (404) |
|
|
|
|
|
beta-Thalassemia [MESH:D017086] (458) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
|
|
Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Glutamine deficiency, congenital [MESH:C536832] (117) |
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (195) |
|
|
Xanthomatosis, Cerebrotendinous [MESH:D019294] (90) |
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
|
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
Acatalasia [MESH:D020642] (788) |
|
|
Bethlem myopathy [MESH:C535436] (108) |
|
|
Muscular dystrophy congenital, merosin negative [MESH:C537384] (34) |
|
|
Scleroatonic muscular dystrophy [MESH:C537521] (108) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Wilms Tumor [MESH:D009396] (553) |
|
|
Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
|
|
Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
|
|
Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
|
|
dowling-degos disease [MESH:C562924] (53) |
|
|
Ichthyosis Vulgaris [MESH:D016112] (27) |
|
|
Dermatitis, Atopic, 2 [MESH:C565293] (26) |
|
|
Dermatitis, Atopic, 1 [MESH:C566404] (26) |
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
|
Steatocystoma Multiplex [MESH:D062685] (56) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
|
|
|
Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150) |
|
|
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, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84) |
|
|
Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62) |
|
|
Keratosis palmoplantaris striata 1 [MESH:C536162] (54) |
|
|
Keratosis palmoplantaris striata 3 [MESH:C536163] (48) |
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
|
Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71) |
|
|
Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75) |
|
|
Asphyxia Neonatorum [MESH:D001238] (1648) |
|
|
Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
|
|
Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48) |
|
|
|
|
|
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84) |
|
|
Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62) |
|
|
Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Scleroderma, Systemic [MESH:D012595] (199) |
|
|
Keloid [MESH:D007627] (1111) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
|
|
Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
|
|
Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452) |
|
|
Scleroderma, Systemic [MESH:D012595] (199) |
|
|
Skin Ulcer [MESH:D012883] (229) |
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
|
|
Eczema [MESH:D004485] (235) |
|
|
Dermatitis, Atopic, 2 [MESH:C565293] (26) |
|
|
Dermatitis, Atopic, 1 [MESH:C566404] (26) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48) |
|
|
Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
Pseudofolliculitis Barbae [MESH:C563016] (16) |
|
|
|
|
|
Dermatopathia pigmentosa reticularis [MESH:C535374] (38) |
|
|
|
|
|
Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48) |
|
|
Ichthyosis Vulgaris [MESH:D016112] (27) |
|
|
|
|
|
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84) |
|
|
Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62) |
|
|
Keratosis palmoplantaris striata 1 [MESH:C536162] (54) |
|
|
Keratosis palmoplantaris striata 3 [MESH:C536163] (48) |
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
|
Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71) |
|
|
Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75) |
|
|
Dermatopathia pigmentosa reticularis [MESH:C535374] (38) |
|
|
Steatocystoma Multiplex [MESH:D062685] (56) |
|
|
|
|
|
Dermatopathia pigmentosa reticularis [MESH:C535374] (38) |
|
|
dowling-degos disease [MESH:C562924] (53) |
|
|
|
|
|
Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48) |
|
|
|
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
|
Steatocystoma Multiplex [MESH:D062685] (56) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
|
|
|
Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150) |
|
|
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 hystrix, Curth Macklin type [MESH:C536088] (48) |
|
|
Ichthyosis Vulgaris [MESH:D016112] (27) |
|
|
|
|
|
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84) |
|
|
Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62) |
|
|
Eczema [MESH:D004485] (235) |
|
|
Dermatitis, Atopic, 2 [MESH:C565293] (26) |
|
|
Dermatitis, Atopic, 1 [MESH:C566404] (26) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48) |
|
|
dowling-degos disease [MESH:C562924] (53) |
|
|
Ichthyosis Vulgaris [MESH:D016112] (27) |
|
|
Dermatitis, Atopic, 2 [MESH:C565293] (26) |
|
|
Dermatitis, Atopic, 1 [MESH:C566404] (26) |
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
|
Steatocystoma Multiplex [MESH:D062685] (56) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
|
|
|
Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150) |
|
|
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, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84) |
|
|
Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62) |
|
|
Keratosis palmoplantaris striata 1 [MESH:C536162] (54) |
|
|
Keratosis palmoplantaris striata 3 [MESH:C536163] (48) |
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
|
Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71) |
|
|
Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75) |
|
|
|
|
|
|
|
|
Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
|
|
dowling-degos disease [MESH:C562924] (53) |
|
|
Psoriasis [MESH:D011565] (3278) |
|
|
Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
|
|
|
|
|
|
Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150) |
|
|
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) |
|
|
Dermatopathia pigmentosa reticularis [MESH:C535374] (38) |
|
|
|
|
|
Naegeli syndrome [MESH:C538331] (38) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
|
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
Calcinosis [MESH:D002114] (2989) |
|
|
Hyperglycemia [MESH:D006943] (1858) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106) |
|
|
Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106) |
|
|
|
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
Xanthomatosis, Cerebrotendinous [MESH:D019294] (90) |
|
|
Celiac Disease [MESH:D002446] (340) |
|
|
|
|
|
Glutamine deficiency, congenital [MESH:C536832] (117) |
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (195) |
|
|
Xanthomatosis, Cerebrotendinous [MESH:D019294] (90) |
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
|
|
|
|
|
|
|
|
|
Gaucher-like disease [MESH:C537675] (17) |
|
|
Gaucher Disease, Perinatal Lethal [MESH:C564306] (17) |
|
|
Acatalasia [MESH:D020642] (788) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
|
|
|
|
|
|
Protein Deficiency [MESH:D011488] (1057) |
|
|
Vitamin A Deficiency [MESH:D014802] (705) |
|
|
Obesity [MESH:D009765] (4462) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
|
|
|
Adrenocortical Carcinoma [MESH:D018268] (821) |
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Adrenocortical Carcinoma [MESH:D018268] (821) |
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Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
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Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
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Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
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Diabetic Cardiomyopathies [MESH:D058065] (1995) |
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Diabetic Neuropathies [MESH:D003929] (2443) |
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Diabetic Retinopathy [MESH:D003930] (1371) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Adrenocortical Carcinoma [MESH:D018268] (821) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Prolactinoma [MESH:D015175] (312) |
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Puberty, Precocious [MESH:D011629] (1147) |
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Ovarian Cysts [MESH:D010048] (2534) |
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Ovarian Neoplasms [MESH:D010051] (3281) |
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Acromegaly [MESH:D000172] (466) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Prolactinoma [MESH:D015175] (312) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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C20. Immune System Diseases |
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C20. Immune System Diseases |
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Arthritis, Rheumatoid [MESH:D001172] (3601) |
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Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
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Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
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Myasthenia Gravis [MESH:D009157] (632) |
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Multiple Sclerosis [MESH:D009103] (1716) |
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Asthma, Aspirin-Induced [MESH:D055963] (1055) |
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Dermatitis, Allergic Contact [MESH:D017449] (3241) |
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Asthma, Aspirin-Induced [MESH:D055963] (1055) |
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Dermatitis, Atopic, 2 [MESH:C565293] (26) |
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Dermatitis, Atopic, 1 [MESH:C566404] (26) |
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Asthma [MESH:D001249] (3914) |
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Angioedema [MESH:D000799] (837) |
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Lymphopenia [MESH:D008231] (990) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Granulomatous Disease, Chronic [MESH:D006105] (404) |
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Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
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Multiple Myeloma [MESH:D009101] (2765) |
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C22. Animal Diseases |
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C22. Animal Diseases |
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Disease Models, Animal [MESH:D004195] (2058) |
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Hepatitis, Animal [MESH:D006520] (260) |
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Mammary Neoplasms, Animal [MESH:D015674] (2735) |
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Dermatopathia pigmentosa reticularis [MESH:C535374] (38) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Hernia, Diaphragmatic [MESH:D006548] (2647) |
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Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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Intestinal Polyps [MESH:D007417] (1592) |
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Arrhythmias, Cardiac [MESH:D001145] (4658) |
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Gliosis [MESH:D005911] (1419) |
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Hemolysis [MESH:D006461] (280) |
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Hyperplasia [MESH:D006965] (2463) |
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Leukocytosis [MESH:D007964] (978) |
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Necrosis [MESH:D009336] (4019) |
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Nerve Degeneration [MESH:D009410] (4061) |
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Micronuclei, Chromosome-Defective [MESH:D048629] (1013) |
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Disease Progression [MESH:D018450] (2868) |
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Disease Susceptibility [MESH:D004198] (1200) |
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Recurrence [MESH:D012008] (830) |
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Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452) |
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Keloid [MESH:D007627] (1110) |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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Fetal Growth Retardation [MESH:D005317] (986) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Hematoma, Epidural, Spinal [MESH:D046748] (167) |
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Hematoma, Subdural [MESH:D006408] (215) |
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Cerebral Hemorrhage [MESH:D002543] (2872) |
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Hematoma, Subdural [MESH:D006408] (212) |
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Neurogenic Inflammation [MESH:D020078] (2246) |
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Bacteremia [MESH:D016470] (1369) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Lymphatic Metastasis [MESH:D008207] (917) |
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Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Scleroatonic muscular dystrophy [MESH:C537521] (108) |
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Shock, Cardiogenic [MESH:D012770] (269) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Edema [MESH:D004487] (3726) |
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Flushing [MESH:D005483] (506) |
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Fever [MESH:D005334] (2856) |
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Weight Gain [MESH:D015430] (2595) |
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Cachexia [MESH:D002100] (2283) |
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Obesity [MESH:D009765] (4454) |
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Paresis [MESH:D010291] (419) |
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Seizures [MESH:D012640] (4502) |
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Hypokinesia [MESH:D018476] (279) |
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Lethargy [MESH:D053609] (1035) |
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Memory Disorders [MESH:D008569] (3233) |
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Learning Disorders [MESH:D007859] (2727) |
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Aphasia [MESH:D001037] (219) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Low Back Pain [MESH:D017116] (244) |
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Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
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Taste Disorders [MESH:D013651] (461) |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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Hyperalgesia [MESH:D006930] (3929) |
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Sleep Deprivation [MESH:D012892] (233) |
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Low Back Pain [MESH:D017116] (244) |
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Acute Coronary Syndrome [MESH:D054058] (2286) |
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Albuminuria [MESH:D000419] (2394) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
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Asthma, Aspirin-Induced [MESH:D055963] (1055) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Manganese Poisoning [MESH:D020149] (2214) |
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Favism [MESH:D005236] (193) |
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Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
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Favism [MESH:D005236] (193) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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C26. Wounds and Injuries |
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C26. Wounds and Injuries |
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Not Fully Specified [NFS] (2454) |
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Burns [MESH:D002056] (2565) |
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Brain Injuries [MESH:D001930] (3431) |
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Hematoma, Subdural [MESH:D006408] (212) |
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Radiation Injuries, Experimental [MESH:D011833] (2662) |
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Spinal Cord Compression [MESH:D013117] (1800) |
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Brain Injuries [MESH:D001930] (3431) |
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Hematoma, Subdural [MESH:D006408] (212) |
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D02. Organic Chemicals |
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D02. Organic Chemicals |
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Tretinoin [MESH:D014212] (83) |
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Tretinoin [MESH:D014212] (83) |
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Tretinoin [MESH:D014212] (83) |
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D23. Biological Factors |
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D23. Biological Factors |
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Tretinoin [MESH:D014212] (83) |
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