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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aldo-keto reductase family 1, member B10 (aldose reductase) [HGNC:AKR1B10] (76) |
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aldo-keto reductase family 1, member C1 [HGNC:AKR1C1] (148) |
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aldo-keto reductase family 1, member C3 [HGNC:AKR1C3] (128) |
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nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [HGNC:NFKBIA] (290) |
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ATP-binding cassette, sub-family C (CFTR/MRP), member 5 [HGNC:ABCC5] (40) |
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inhibitor of DNA binding 1, dominant negative helix-loop-helix protein [HGNC:ID1] (63) |
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MAX dimerization protein 1 [HGNC:MXD1] (46) |
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nuclear factor, erythroid 2-like 2 [HGNC:NFE2L2] (213) |
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thrombomodulin [HGNC:THBD] (38) |
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chemokine (C-C motif) ligand 02 [HGNC:CCL2] (337) |
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chemokine (C-C motif) ligand 26 [HGNC:CCL26] (13) |
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chemokine (C-C motif) ligand 02 [HGNC:CCL2] (337) |
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chemokine (C-C motif) ligand 26 [HGNC:CCL26] (13) |
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chemokine (C-X-C motif) ligand 01 (melanoma growth stimulating activity, alpha) [HGNC:CXCL1] (82) |
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chemokine (C-X-C motif) ligand 02 [HGNC:CXCL2] (65) |
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chemokine (C-X-C motif) ligand 03 [HGNC:CXCL3] (43) |
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interleukin 08 [HGNC:IL8] (649) |
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angiopoietin-like 4 [HGNC:ANGPTL4] (40) |
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glutathione S-transferase pi 1 [HGNC:GSTP1] (218) |
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heat shock 70kDa protein 01A [HGNC:HSPA1A] (112) |
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heat shock 70kDa protein 01-like [HGNC:HSPA1L] (36) |
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high mobility group AT-hook 2 [HGNC:HMGA2] (21) |
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IKAROS family zinc finger 4 (Eos) [HGNC:IKZF4] (1) |
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interferon, gamma [HGNC:IFNG] (274) |
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interleukin 06 (interferon, beta 2) [HGNC:IL6] (511) |
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interleukin 01, beta [HGNC:IL1B] (497) |
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interleukin 02 [HGNC:IL2] (144) |
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interleukin 06 (interferon, beta 2) [HGNC:IL6] (511) |
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interleukin 07 [HGNC:IL7] (23) |
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interleukin 08 [HGNC:IL8] (649) |
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interleukin 10 [HGNC:IL10] (187) |
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interleukin 11 [HGNC:IL11] (44) |
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interleukin 24 [HGNC:IL24] (37) |
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lysine (K)-specific methyltransferase 2A [HGNC:KMT2A] (22) |
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MAX dimerization protein 1 [HGNC:MXD1] (46) |
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growth arrest-specific 5 (non-protein coding) [HGNC:GAS5] (8) |
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tumor necrosis factor, alpha-induced protein 3 [HGNC:TNFAIP3] (88) |
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lysine (K)-specific methyltransferase 2A [HGNC:KMT2A] (22) |
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myosin phosphatase Rho interacting protein [HGNC:MPRIP] (16) |
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prostaglandin E receptor 4 (subtype EP4) [HGNC:PTGER4] (20) |
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dual specificity phosphatase 10 [HGNC:DUSP10] (34) |
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SRY (sex determining region Y)-box 09 [HGNC:SOX9] (39) |
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trafficking protein particle complex 10 [HGNC:TRAPPC10] (6) |
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tumor necrosis factor [HGNC:TNF] (795) |
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GLI family zinc finger 2 [HGNC:GLI2] (15) |
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IKAROS family zinc finger 4 (Eos) [HGNC:IKZF4] (1) |
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zinc finger, MIZ-type containing 1 [HGNC:ZMIZ1] (19) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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binding (2423) |
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localization (731) |
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metabolic processing (485) |
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activity (2549) |
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expression (2187) |
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reaction (3393) |
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response to substance (713) |
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secretion (346) |
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expression (3238) |
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metabolic processing (740) |
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reaction (1574) |
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reduction (162) |
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response to substance (641) |
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A. Anatomy |
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A. Anatomy |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Chlamydia Infections [MESH:D002690] (1696) |
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Salmonella Infections, Animal [MESH:D012481] (604) |
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Legionnaires' Disease [MESH:D007877] (611) |
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Listeriosis [MESH:D008088] (1622) |
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Tuberculosis, Pulmonary [MESH:D014397] (678) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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Appendicitis [MESH:D001064] (774) |
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Peritonitis [MESH:D010538] (800) |
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Shock, Septic [MESH:D012772] (1830) |
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Chlamydia Infections [MESH:D002690] (1693) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Meningitis, Aseptic [MESH:D008582] (1305) |
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Hepatitis B [MESH:D006509] (976) |
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Sarcoma, Kaposi [MESH:D012514] (1578) |
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Hepatitis B [MESH:D006509] (976) |
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Hepatitis C [MESH:D006526] (1627) |
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Meningitis, Aseptic [MESH:D008582] (1305) |
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Hepatitis C [MESH:D006526] (1627) |
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Respiratory Syncytial Virus Infections [MESH:D018357] (852) |
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Influenza, Human [MESH:D007251] (1075) |
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Cardiovirus Infections [MESH:D018188] (1548) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Trichuriasis [MESH:D014257] (805) |
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Malaria [MESH:D008288] (2175) |
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Entamoebiasis [MESH:D004749] (1689) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
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Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
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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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Precancerous Conditions [MESH:D011230] (2858) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
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Leukemia, Myelomonocytic, Acute [MESH:D015479] (85) |
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Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344) |
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Leukemia, Monocytic, Acute [MESH:D007948] (98) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Lymphoma, AIDS-Related [MESH:D016483] (278) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Liposarcoma, Myxoid [MESH:D018208] (358) |
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Mastocytosis, Systemic [MESH:D034721] (769) |
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Osteosarcoma [MESH:D012516] (2175) |
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Fibromatosis, Aggressive [MESH:D018222] (1562) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Osteosarcoma [MESH:D012516] (2175) |
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Sarcoma, Kaposi [MESH:D012514] (1578) |
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Liposarcoma, Myxoid [MESH:D018208] (358) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Mesothelioma [MESH:D008654] (2567) |
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Oncocytoma, renal [MESH:C537750] (35) |
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Carcinoma, Lewis Lung [MESH:D018827] (248) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Cholangiocarcinoma [MESH:D018281] (2398) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Mesothelioma [MESH:D008654] (2567) |
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Glioblastoma [MESH:D005909] (2554) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Papilloma [MESH:D010212] (2243) |
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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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Sarcoma, Kaposi [MESH:D012514] (1578) |
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Melanoma [MESH:D008545] (3508) |
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Breast Neoplasms [MESH:D001943] (6077) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Soft Tissue Neoplasms [MESH:D012983] (2003) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Bone Marrow Neoplasms [MESH:D019046] (91) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Brain Neoplasms [MESH:D001932] (2764) |
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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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Vaginal Neoplasms [MESH:D014625] (363) |
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Endometrial Neoplasms [MESH:D016889] (1987) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Oncocytoma, renal [MESH:C537750] (35) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Carcinoma, Lewis Lung [MESH:D018827] (248) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm, Residual [MESH:D018365] (478) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Lymphatic Metastasis [MESH:D008207] (917) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Birt-Hogg-Dube Syndrome [MESH:D058249] (35) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Osteitis Deformans [MESH:D010001] (287) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Klippel Feil syndrome dominant type [MESH:C536887] (8) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Osteolysis [MESH:D010014] (1787) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Spondylitis, Ankylosing [MESH:D013167] (431) |
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Hand Deformities, Congenital [MESH:D006228] (587) |
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Pierre Robin Syndrome [MESH:D010855] (101) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Arthralgia [MESH:D018771] (191) |
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Spondylitis, Ankylosing [MESH:D013167] (431) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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Arthritis, Juvenile [MESH:D001171] (1060) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Osteoarthritis [MESH:D010003] (1743) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Spondylitis, Ankylosing [MESH:D013167] (431) |
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Muscle Weakness [MESH:D018908] (478) |
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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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Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
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Dermatomyositis [MESH:D003882] (1826) |
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Dermatomyositis [MESH:D003882] (1826) |
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Campomelic Dysplasia [MESH:D055036] (75) |
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Microcephaly [MESH:D008831] (700) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Pierre Robin Syndrome [MESH:D010855] (101) |
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Klippel Feil syndrome dominant type [MESH:C536887] (8) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Hand Deformities, Congenital [MESH:D006228] (587) |
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Arthritis, Juvenile [MESH:D001171] (1060) |
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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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Cholestasis [MESH:D002779] (3419) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Gastrointestinal Hemorrhage [MESH:D006471] (815) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Gastroesophageal Reflux [MESH:D005764] (1465) |
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Eosinophilic Esophagitis [MESH:D057765] (43) |
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Esophagitis, Peptic [MESH:D004942] (709) |
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Appendicitis [MESH:D001064] (774) |
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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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Eosinophilic Esophagitis [MESH:D057765] (43) |
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Esophagitis, Peptic [MESH:D004942] (709) |
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Gastritis, Atrophic [MESH:D005757] (947) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Appendicitis [MESH:D001064] (774) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Irritable Bowel Syndrome [MESH:D043183] (429) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Peptic Ulcer [MESH:D010437] (1969) |
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Enterocolitis, Necrotizing [MESH:D020345] (1367) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
|
|
Cecal Neoplasms [MESH:D002430] (822) |
|
|
Colonic Neoplasms [MESH:D003110] (4405) |
|
|
Celiac Disease [MESH:D002446] (340) |
|
|
Colorectal Neoplasms [MESH:D015179] (4534) |
|
|
Esophagitis, Peptic [MESH:D004942] (709) |
|
|
Stomach Ulcer [MESH:D013276] (2915) |
|
|
Gastroparesis [MESH:D018589] (732) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Gastritis, Atrophic [MESH:D005757] (947) |
|
|
Stomach Ulcer [MESH:D013276] (2915) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Hepatic Veno-Occlusive Disease [MESH:D006504] (208) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
|
|
|
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
Liver Failure, Acute [MESH:D017114] (2404) |
|
|
Hepatitis, Alcoholic [MESH:D006519] (1613) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Hepatitis B [MESH:D006509] (976) |
|
|
Hepatitis C [MESH:D006526] (1627) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
|
|
Hepatitis, Alcoholic [MESH:D006519] (1613) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
|
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Peritonitis [MESH:D010538] (800) |
|
 |
C07. Stomatognathic Diseases |
 |
 |
|
C07. Stomatognathic Diseases |
|
|
|
|
|
|
|
|
Pierre Robin Syndrome [MESH:D010855] (101) |
|
|
|
|
|
Basal Cell Nevus Syndrome [MESH:D001478] (67) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Mucositis [MESH:D052016] (1238) |
|
|
Oral Submucous Fibrosis [MESH:D009914] (2432) |
|
|
Stomatitis [MESH:D013280] (1235) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
|
|
|
|
|
|
Pierre Robin Syndrome [MESH:D010855] (101) |
|
 |
C08. Respiratory Tract Diseases |
 |
 |
|
C08. Respiratory Tract Diseases |
|
|
Not Fully Specified [NFS] (1984) |
|
|
|
|
|
Asthma [MESH:D001249] (4098) |
|
|
Bronchial Hyperreactivity [MESH:D016535] (1357) |
|
|
Bronchiectasis [MESH:D001987] (1792) |
|
|
|
|
|
Bronchiolitis Obliterans [MESH:D001989] (611) |
|
|
Pneumonia [MESH:D011014] (3482) |
|
|
Pulmonary Edema [MESH:D011654] (2109) |
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Pulmonary Fibrosis [MESH:D011658] (3140) |
|
|
Pulmonary Veno-Occlusive Disease [MESH:D011668] (55) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
Pulmonary arterial hypertension [MESH:C536282] (94) |
|
|
|
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Asthma [MESH:D001249] (3903) |
|
|
|
|
|
Bronchiolitis Obliterans [MESH:D001989] (611) |
|
|
Pulmonary Emphysema [MESH:D011656] (1259) |
|
|
|
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Pneumothorax, Primary Spontaneous [MESH:C566795] (35) |
|
|
Cough [MESH:D003371] (179) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
Asthma [MESH:D001249] (4098) |
|
|
Influenza, Human [MESH:D007251] (1075) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Pneumonia [MESH:D011014] (3482) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
Legionnaires' Disease [MESH:D007877] (611) |
|
|
|
|
|
|
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
 |
C09. Otorhinolaryngologic Diseases |
 |
 |
|
C09. Otorhinolaryngologic Diseases |
|
|
|
|
|
|
|
|
Vestibular Diseases [MESH:D015837] (819) |
|
 |
C10. Nervous System Diseases |
 |
 |
|
C10. Nervous System Diseases |
|
|
Not Fully Specified [NFS] (4027) |
|
|
Sleep Disorders [MESH:D012893] (2050) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
Brain Neoplasms [MESH:D001932] (2764) |
|
|
|
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
Maple Syrup Urine Disease [MESH:D008375] (127) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
|
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
|
|
|
Migraine Disorders [MESH:D008881] (2318) |
|
|
|
|
|
|
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
|
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
|
|
|
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) |
|
|
|
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
|
|
|
Charcot-Marie-Tooth Disease, Type 4H [MESH:C563740] (29) |
|
|
Microcephaly [MESH:D008831] (700) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
Brain Neoplasms [MESH:D001932] (2764) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
von Hippel-Lindau Disease [MESH:D006623] (580) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
|
|
|
Charcot-Marie-Tooth Disease, Type 4H [MESH:C563740] (29) |
|
|
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) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Ataxia [MESH:D001259] (1138) |
|
|
Hyperkinesis [MESH:D006948] (1799) |
|
|
Tremor [MESH:D014202] (840) |
|
|
Lethargy [MESH:D053609] (1035) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Martsolf syndrome [MESH:C536028] (21) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Muscle Weakness [MESH:D018908] (478) |
|
|
Headache [MESH:D006261] (1416) |
|
|
Pain, Intractable [MESH:D010148] (707) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
|
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
|
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
|
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth Disease, Type 4H [MESH:C563740] (29) |
|
|
|
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
Eyelid Diseases [MESH:D005141] (882) |
|
|
Coloboma [MESH:D003103] (315) |
|
|
Microphthalmia, Isolated 4 [MESH:C567757] (8) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Martsolf syndrome [MESH:C536028] (21) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
|
|
|
|
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Hypospadias [MESH:D007021] (798) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Prostatitis [MESH:D011472] (424) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
Hypospadias [MESH:D007021] (798) |
|
|
|
|
|
Hyperandrogenism [MESH:D017588] (98) |
|
|
Hyperandrogenism [MESH:D017588] (98) |
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Oncocytoma, renal [MESH:C537750] (35) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Oncocytoma, renal [MESH:C537750] (35) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Glomerulonephritis [MESH:D005921] (3758) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
|
|
|
Atypical hemolytic uremic syndrome [MESH:C538266] (277) |
|
|
Cystitis [MESH:D003556] (604) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Urinary Bladder, Overactive [MESH:D053201] (530) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
 |
C13. Female Urogenital Diseases and Pregnancy Complications |
 |
 |
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
|
|
|
Endometriosis [MESH:D004715] (2461) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
Vaginal Neoplasms [MESH:D014625] (363) |
|
|
Hypospadias [MESH:D007021] (798) |
|
|
|
|
|
Hyperandrogenism [MESH:D017588] (98) |
|
|
Hyperandrogenism [MESH:D017588] (98) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Vaginal Neoplasms [MESH:D014625] (363) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Oncocytoma, renal [MESH:C537750] (35) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Oncocytoma, renal [MESH:C537750] (35) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Glomerulonephritis [MESH:D005921] (3758) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
|
|
|
Atypical hemolytic uremic syndrome [MESH:C538266] (277) |
|
|
Cystitis [MESH:D003556] (604) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Urinary Bladder, Overactive [MESH:D053201] (530) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Placenta Diseases [MESH:D010922] (1781) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Pre-Eclampsia [MESH:D011225] (1435) |
|
|
Obstetric Labor, Premature [MESH:D007752] (1316) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
|
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Heart Valve Diseases [MESH:D006349] (3333) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocarditis [MESH:D009205] (1708) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Ventricular Dysfunction, Left [MESH:D018487] (1631) |
|
|
Diabetic Angiopathies [MESH:D003925] (1984) |
|
|
Hepatic Veno-Occlusive Disease [MESH:D006504] (208) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypertension [MESH:D006973] (5655) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Pulmonary Veno-Occlusive Disease [MESH:D011668] (55) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
von Hippel-Lindau Disease [MESH:D006623] (580) |
|
|
|
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
|
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Venous Thrombosis [MESH:D020246] (1141) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
Pancytopenia [MESH:D010198] (332) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
|
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Bone Marrow failure syndromes [MESH:C536572] (248) |
|
|
Atypical hemolytic uremic syndrome [MESH:C538266] (277) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
|
|
|
Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
|
|
|
|
|
|
|
|
|
|
|
Atypical hemolytic uremic syndrome [MESH:C538266] (277) |
|
|
Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
|
|
|
|
|
Hypoalbuminemia [MESH:D034141] (1332) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Bone Marrow Neoplasms [MESH:D019046] (91) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
Bone Marrow failure syndromes [MESH:C536572] (248) |
|
|
Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
|
|
Bone Marrow Neoplasms [MESH:D019046] (91) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Leukocytosis [MESH:D007964] (988) |
|
|
Eosinophilic Esophagitis [MESH:D057765] (43) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
Job Syndrome [MESH:D007589] (772) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
|
|
|
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) |
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
|
|
|
Lymphoma, AIDS-Related [MESH:D016483] (278) |
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
|
|
|
Basal Cell Nevus Syndrome [MESH:D001478] (67) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
|
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
Coloboma [MESH:D003103] (315) |
|
|
Microphthalmia, Isolated 4 [MESH:C567757] (8) |
|
|
Campomelic Dysplasia [MESH:D055036] (75) |
|
|
Microcephaly [MESH:D008831] (700) |
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
|
|
|
Pierre Robin Syndrome [MESH:D010855] (101) |
|
|
Klippel Feil syndrome dominant type [MESH:C536887] (8) |
|
|
Hand Deformities, Congenital [MESH:D006228] (587) |
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
|
|
|
|
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
|
|
|
Charcot-Marie-Tooth Disease, Type 4H [MESH:C563740] (29) |
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
Microcephaly [MESH:D008831] (700) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
|
|
|
|
|
|
Pierre Robin Syndrome [MESH:D010855] (101) |
|
|
Hypospadias [MESH:D007021] (798) |
|
|
|
|
|
Hyperandrogenism [MESH:D017588] (98) |
|
|
Hyperandrogenism [MESH:D017588] (98) |
|
|
|
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
|
|
|
Charcot-Marie-Tooth Disease, Type 4H [MESH:C563740] (29) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
Maple Syrup Urine Disease [MESH:D008375] (127) |
|
|
Maple Syrup Urine Disease [MESH:D008375] (127) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
De Vivo disease [MESH:C536830] (172) |
|
|
|
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Basal Cell Nevus Syndrome [MESH:D001478] (67) |
|
|
Birt-Hogg-Dube Syndrome [MESH:D058249] (35) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
|
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
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, Localized [MESH:D012594] (1597) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
Chloracne [MESH:D054506] (1274) |
|
|
Breast Neoplasms [MESH:D001943] (6077) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
|
|
|
Alopecia Areata [MESH:D000506] (168) |
|
|
|
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
|
|
|
Vitiligo [MESH:D014820] (504) |
|
|
|
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
|
|
|
|
|
|
|
|
|
Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
|
|
Lichenoid Eruptions [MESH:D017512] (1324) |
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
Maple Syrup Urine Disease [MESH:D008375] (127) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Calcinosis [MESH:D002114] (2989) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hyperglycemia [MESH:D006943] (1858) |
|
|
Hypoglycemia [MESH:D007003] (2420) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
Hyperlipidemias [MESH:D006949] (1908) |
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
Celiac Disease [MESH:D002446] (340) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
Maple Syrup Urine Disease [MESH:D008375] (127) |
|
|
Maple Syrup Urine Disease [MESH:D008375] (127) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
De Vivo disease [MESH:C536830] (172) |
|
|
|
|
|
Sjogren-Larsson Syndrome [MESH:D016111] (67) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
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) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Hypokalemia [MESH:D007008] (1041) |
|
|
Hyponatremia [MESH:D007010] (789) |
|
|
|
|
|
|
|
|
Protein Deficiency [MESH:D011488] (1057) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
Obesity [MESH:D009765] (4462) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetic Angiopathies [MESH:D003925] (1984) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
|
|
|
|
|
|
Hyperandrogenism [MESH:D017588] (98) |
|
|
Hyperandrogenism [MESH:D017588] (98) |
|
|
Martsolf syndrome [MESH:C536028] (21) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
|
|
|
Hyperparathyroidism, Secondary [MESH:D006962] (1138) |
|
|
|
|
|
Holoprosencephaly 9 [MESH:C563659] (35) |
|
|
Hyperthyroidism [MESH:D006980] (1191) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
Graft vs Host Disease [MESH:D006086] (674) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Drug Hypersensitivity [MESH:D004342] (4000) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Eosinophilic Esophagitis [MESH:D057765] (43) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Job Syndrome [MESH:D007589] (772) |
|
|
|
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) |
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
|
|
|
Lymphoma, AIDS-Related [MESH:D016483] (278) |
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
 |
C22. Animal Diseases |
 |
 |
|
C22. Animal Diseases |
|
|
Disease Models, Animal [MESH:D004195] (2058) |
|
|
Mammary Neoplasms, Animal [MESH:D015674] (2735) |
|
|
Salmonella Infections, Animal [MESH:D012481] (604) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
|
|
|
Hernia, Diaphragmatic [MESH:D006548] (2647) |
|
|
Cardiomegaly [MESH:D006332] (3802) |
|
|
Anonychia congenita [MESH:C536377] (69) |
|
|
Intestinal Polyps [MESH:D007417] (1592) |
|
|
Chromosome Aberrations [MESH:D002869] (2352) |
|
|
Emphysema [MESH:D004646] (1096) |
|
|
Fibrosis [MESH:D005355] (3133) |
|
|
Growth Disorders [MESH:D006130] (2438) |
|
|
Hyperbilirubinemia [MESH:D006932] (1860) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Leukocytosis [MESH:D007964] (978) |
|
|
Muscle Weakness [MESH:D018908] (478) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
Ulcer [MESH:D014456] (392) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Genetic Predisposition to Disease [MESH:D020022] (966) |
|
|
Gastrointestinal Hemorrhage [MESH:D006471] (815) |
|
|
Shock, Hemorrhagic [MESH:D012771] (2042) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2872) |
|
|
|
|
|
Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
|
|
|
Shock, Septic [MESH:D012772] (1830) |
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Infarction [MESH:D007238] (298) |
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Infarction [MESH:D007238] (298) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm, Residual [MESH:D018365] (478) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Lymphatic Metastasis [MESH:D008207] (917) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Multiple Organ Failure [MESH:D009102] (1836) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Shock, Septic [MESH:D012772] (1830) |
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Asthenia [MESH:D001247] (376) |
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Chills [MESH:D023341] (644) |
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Edema [MESH:D004487] (3726) |
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Fever [MESH:D005334] (2856) |
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Hypothermia [MESH:D007035] (2075) |
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Birth Weight [MESH:D001724] (377) |
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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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Seizures [MESH:D012640] (4502) |
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Sleep Disorders [MESH:D012893] (1301) |
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Ataxia [MESH:D001259] (984) |
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Hyperkinesis [MESH:D006948] (1799) |
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Tremor [MESH:D014202] (840) |
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Lethargy [MESH:D053609] (1035) |
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Learning Disorders [MESH:D007859] (2727) |
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Amnesia [MESH:D000647] (1911) |
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Martsolf syndrome [MESH:C536028] (21) |
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Muscle Weakness [MESH:D018908] (478) |
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Headache [MESH:D006261] (1417) |
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Pain, Intractable [MESH:D010148] (707) |
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Neuralgia, Postherpetic [MESH:D051474] (742) |
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Gastroparesis [MESH:D018589] (732) |
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Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
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Hyperalgesia [MESH:D006930] (3929) |
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Arthralgia [MESH:D018771] (191) |
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Headache [MESH:D006261] (1417) |
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Pain, Intractable [MESH:D010148] (707) |
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Acute Coronary Syndrome [MESH:D054058] (2286) |
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Angina, Unstable [MESH:D000789] (782) |
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Angina, Stable [MESH:D060050] (1702) |
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Neuralgia, Postherpetic [MESH:D051474] (742) |
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Anorexia [MESH:D000855] (854) |
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Diarrhea [MESH:D003967] (858) |
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Nausea [MESH:D009325] (2300) |
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Vomiting [MESH:D014839] (1354) |
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Cough [MESH:D003371] (179) |
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Respiratory Sounds [MESH:D012135] (713) |
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Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
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Urinary Bladder, Overactive [MESH:D053201] (530) |
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Albuminuria [MESH:D000419] (2394) |
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C24. Occupational Diseases |
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C24. Occupational Diseases |
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Berylliosis [MESH:D001607] (2005) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug Hypersensitivity [MESH:D004342] (4001) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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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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Neurotoxicity Syndromes [MESH:D020258] (3323) |
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Psychoses, Substance-Induced [MESH:D011605] (2053) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Psychoses, Substance-Induced [MESH:D011605] (2052) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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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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Heat Stress Disorders [MESH:D018882] (226) |
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Vascular System Injuries [MESH:D057772] (2086) |
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Brain Injuries [MESH:D001930] (3431) |
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Radiation Injuries, Experimental [MESH:D011833] (2662) |
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Spinal Cord Compression [MESH:D013117] (1800) |
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Lung Injury [MESH:D055370] (1814) |
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Brain Injuries [MESH:D001930] (3431) |
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D02. Organic Chemicals |
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D02. Organic Chemicals |
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Aldehydes [MESH:D000447] (756) |
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F. Psychiatry and Psychology |
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F. Psychiatry and Psychology |
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Martsolf syndrome [MESH:C536028] (21) |
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Martsolf syndrome [MESH:C536028] (21) |
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