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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ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355) |
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ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355) |
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integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) [HGNC:ITGA2] (42) |
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integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) [HGNC:ITGB3] (49) |
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chemokine (C-C motif) ligand 04 [HGNC:CCL4] (96) |
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chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141) |
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cytochrome P450, family 01, subfamily A, polypeptide 02 [HGNC:CYP1A2] (466) |
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cytochrome P450, family 02, subfamily B, polypeptide 06 [HGNC:CYP2B6] (216) |
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cytochrome P450, family 02, subfamily C, polypeptide 08 [HGNC:CYP2C8] (106) |
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cytochrome P450, family 02, subfamily C, polypeptide 09 [HGNC:CYP2C9] (220) |
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cytochrome P450, family 02, subfamily C, polypeptide 19 [HGNC:CYP2C19] (172) |
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cytochrome P450, family 02, subfamily D, polypeptide 06 [HGNC:CYP2D6] (200) |
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cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612) |
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cytochrome P450, family 03, subfamily A, polypeptide 05 [HGNC:CYP3A5] (134) |
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chemokine (C-C motif) ligand 04 [HGNC:CCL4] (96) |
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chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141) |
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integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) [HGNC:ITGA2] (42) |
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integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) [HGNC:ITGB3] (49) |
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interleukin 06 (interferon, beta 2) [HGNC:IL6] (511) |
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interleukin 06 (interferon, beta 2) [HGNC:IL6] (511) |
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paraoxonase 1 [HGNC:PON1] (115) |
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coagulation factor II (thrombin) receptor [HGNC:F2R] (49) |
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purinergic receptor P2Y, G-protein coupled, 12 [HGNC:P2RY12] (6) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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abundance (136) |
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binding (2423) |
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cotreatment (1499) |
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phosphorylation (55) |
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reaction (624) |
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response to substance (623) |
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activity (2549) |
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expression (2187) |
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metabolic processing (88) |
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reaction (3393) |
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response to substance (713) |
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secretion (346) |
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uptake (71) |
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activity (2865) |
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cleavage (666) |
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degradation (347) |
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expression (3238) |
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metabolic processing (740) |
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oxidation (295) |
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reaction (1574) |
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response to substance (641) |
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secretion (901) |
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A. Anatomy |
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A. Anatomy |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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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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Listeriosis [MESH:D008088] (1622) |
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Paratuberculosis [MESH:D010283] (427) |
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Tuberculosis, Bovine [MESH:D014380] (380) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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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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Sarcoma, Kaposi [MESH:D012514] (1578) |
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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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Cardiovirus Infections [MESH:D018188] (1548) |
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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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Liver Diseases, Parasitic [MESH:D008109] (1009) |
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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, Cutaneous [MESH:D016773] (2359) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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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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Precancerous Conditions [MESH:D011230] (2858) |
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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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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Carcinosarcoma [MESH:D002296] (581) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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Osteosarcoma [MESH:D012516] (2175) |
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Fibromatosis, Aggressive [MESH:D018222] (1562) |
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Carcinosarcoma [MESH:D002296] (581) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Osteosarcoma [MESH:D012516] (2175) |
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Sarcoma, Kaposi [MESH:D012514] (1578) |
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Gliosarcoma [MESH:D018316] (880) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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Melanoma [MESH:D008545] (3508) |
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Adenoma [MESH:D000236] (4051) |
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Carcinoma, Basal Cell [MESH:D002280] (1628) |
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Carcinoma, Small Cell [MESH:D018288] (1317) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adenocarcinoma, Clear Cell [MESH:D018262] (1291) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Cholangiocarcinoma [MESH:D018281] (2398) |
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Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
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Carcinoma, Basal Cell [MESH:D002280] (1628) |
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Gliosarcoma [MESH:D018316] (880) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Papilloma [MESH:D010212] (2243) |
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Gliosarcoma [MESH:D018316] (880) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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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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Bone Neoplasms [MESH:D001859] (1334) |
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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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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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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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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, Hereditary [MESH:C565972] (769) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Nasopharyngeal carcinoma [MESH:C538339] (1198) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Papilloma, Choroid Plexus [MESH:D020288] (769) |
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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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Penile Neoplasms [MESH:D010412] (890) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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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, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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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 Metastasis [MESH:D009362] (4441) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Li-Fraumeni Syndrome [MESH:D016864] (859) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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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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Acromicric dysplasia [MESH:C535662] (520) |
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Marfan Syndrome [MESH:D008382] (646) |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
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Camurati-Engelmann Syndrome [MESH:D003966] (492) |
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Osteopetrosis [MESH:D010022] (318) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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Intervertebral disc disease [MESH:C535531] (514) |
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Intervertebral disc disease [MESH:C535531] (514) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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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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Compartment Syndromes [MESH:D003161] (80) |
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Mitochondrial Myopathies [MESH:D017240] (2176) |
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Muscle Rigidity [MESH:D009127] (617) |
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Rhabdomyolysis [MESH:D012206] (465) |
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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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Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
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Acromicric dysplasia [MESH:C535662] (520) |
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Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
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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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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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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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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Inflammatory Bowel Disease 13 [MESH:C567384] (435) |
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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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Peptic Ulcer Hemorrhage [MESH:D010438] (553) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Inflammatory Bowel Disease 13 [MESH:C567384] (435) |
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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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Colonic Neoplasms [MESH:D003110] (4405) |
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Colorectal Neoplasms [MESH:D015179] (4534) |
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Hemorrhoids [MESH:D006484] (166) |
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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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Stomach Ulcer [MESH:D013276] (2915) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Hepatic Veno-Occlusive Disease [MESH:D006504] (208) |
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Hepatomegaly [MESH:D006529] (1169) |
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Liver Diseases, Parasitic [MESH:D008109] (1009) |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
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Hepatic Encephalopathy [MESH:D006501] (1795) |
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Liver Failure, Acute [MESH:D017114] (2404) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Hepatitis C [MESH:D006526] (1627) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Cystic Fibrosis [MESH:D003550] (760) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Pancreatitis [MESH:D010195] (1924) |
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Peritoneal Fibrosis [MESH:D056627] (488) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Behcet Syndrome [MESH:D001528] (1784) |
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Oral Submucous Fibrosis [MESH:D009914] (2432) |
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Periodontitis [MESH:D010518] (843) |
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Gingival Hyperplasia [MESH:D005885] (161) |
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Nasopharyngeal carcinoma [MESH:C538339] (1198) |
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Nasopharyngeal carcinoma [MESH:C538339] (1198) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Not Fully Specified [NFS] (1984) |
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Asthma [MESH:D001249] (4098) |
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Bronchial Hyperreactivity [MESH:D016535] (1357) |
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Bronchiectasis [MESH:D001987] (1792) |
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Cystic Fibrosis [MESH:D003550] (760) |
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Hypertension, Pulmonary [MESH:D006976] (2000) |
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Pneumonia [MESH:D011014] (3482) |
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Pulmonary Edema [MESH:D011654] (2109) |
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Pulmonary Embolism [MESH:D011655] (1118) |
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Pulmonary Fibrosis [MESH:D011658] (3140) |
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Surfactant Metabolism Dysfunction, Pulmonary, 1 [MESH:C566882] (102) |
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Anthracosis [MESH:D055008] (1805) |
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Berylliosis [MESH:D001607] (2005) |
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Asthma [MESH:D001249] (3903) |
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Pulmonary Emphysema [MESH:D011656] (1259) |
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Acute Lung Injury [MESH:D055371] (1907) |
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Anthracosis [MESH:D055008] (1805) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
|
Surfactant Metabolism Dysfunction, Pulmonary, 1 [MESH:C566882] (102) |
|
|
|
|
|
Sinusitis [MESH:D012852] (469) |
|
|
|
|
|
Allergic Rhinitis [MESH:C567078] (181) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Dyspnea [MESH:D004417] (248) |
|
|
|
|
|
|
|
|
Congenital central hypoventilation syndrome [MESH:C536209] (341) |
|
|
|
|
|
Congenital central hypoventilation syndrome [MESH:C536209] (341) |
|
|
Ige Responsiveness, Atopic [MESH:C564133] (267) |
|
|
Asthma [MESH:D001249] (4098) |
|
|
Allergic Rhinitis [MESH:C567078] (181) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Pneumonia [MESH:D011014] (3482) |
|
|
Rhinitis [MESH:D012220] (766) |
|
|
Sinusitis [MESH:D012852] (469) |
|
|
|
|
|
|
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
 |
C09. Otorhinolaryngologic Diseases |
 |
 |
|
C09. Otorhinolaryngologic Diseases |
|
|
|
|
|
|
|
|
|
|
|
Deafness [MESH:D003638] (623) |
|
|
|
|
|
Sinusitis [MESH:D012852] (469) |
|
|
|
|
|
Allergic Rhinitis [MESH:C567078] (181) |
|
|
|
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
|
|
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
 |
C10. Nervous System Diseases |
 |
 |
|
C10. Nervous System Diseases |
|
|
Not Fully Specified [NFS] (4027) |
|
|
|
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
|
|
|
Hypotension, Orthostatic [MESH:D007024] (679) |
|
|
|
|
|
Brain Edema [MESH:D001929] (1165) |
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
Idiopathic basal ganglia calcification 1 [MESH:C536275] (139) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
|
|
|
3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32) |
|
|
|
|
|
|
|
|
Papilloma, Choroid Plexus [MESH:D020288] (769) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
Vertebrobasilar Insufficiency [MESH:D014715] (9) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Carotid Artery Thrombosis [MESH:D002341] (138) |
|
|
Carotid Stenosis [MESH:D016893] (174) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
|
|
|
Sinus Thrombosis, Intracranial [MESH:D012851] (356) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
Hematoma, Subdural [MESH:D006408] (212) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
Epilepsy, Tonic-Clonic [MESH:D004830] (1042) |
|
|
|
|
|
Migraine Disorders [MESH:D008881] (2318) |
|
|
|
|
|
|
|
|
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) |
|
|
Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239) |
|
|
Spinal Cord Ischemia [MESH:D020760] (12) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Papilloma, Choroid Plexus [MESH:D020288] (769) |
|
|
Idiopathic basal ganglia calcification 1 [MESH:C536275] (139) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Dystonia [MESH:D004421] (848) |
|
|
Tremor [MESH:D014202] (840) |
|
|
|
|
|
|
|
|
Coma [MESH:D003128] (524) |
|
|
Syncope [MESH:D013575] (128) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Hallucinations [MESH:D006212] (251) |
|
|
|
|
|
Muscle Rigidity [MESH:D009127] (617) |
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Headache [MESH:D006261] (1416) |
|
|
Neuralgia [MESH:D009437] (2074) |
|
|
|
|
|
|
|
|
Deafness [MESH:D003638] (623) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
Hypesthesia [MESH:D006987] (58) |
|
|
Ageusia [MESH:D000370] (20) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239) |
|
|
Mitochondrial Myopathies [MESH:D017240] (2176) |
|
|
|
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Diabetic Neuropathies [MESH:D003929] (2442) |
|
|
Neuralgia [MESH:D009437] (2078) |
|
|
|
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Congenital central hypoventilation syndrome [MESH:C536209] (341) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
|
Hematoma, Subdural [MESH:D006408] (212) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Dry Eye Syndromes [MESH:D015352] (533) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Retinal Vein Occlusion [MESH:D012170] (607) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Infertility, Male [MESH:D007248] (2851) |
|
|
Penile Induration [MESH:D010411] (495) |
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Balkan Nephropathy [MESH:D001449] (772) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
|
|
|
|
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
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) |
|
|
Primary Ovarian Insufficiency [MESH:D016649] (270) |
|
|
Infertility, Female [MESH:D007247] (2184) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
Vulvar Lichen Sclerosus [MESH:D007724] (825) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Balkan Nephropathy [MESH:D001449] (772) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
|
|
|
|
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Placenta Diseases [MESH:D010922] (1781) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Obstetric Labor, Premature [MESH:D007752] (1316) |
|
|
Prenatal Exposure Delayed Effects [MESH:D011297] (870) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
|
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Cardiomegaly [MESH:D006332] (4081) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
|
|
|
Torsades de Pointes [MESH:D016171] (880) |
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1516) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocarditis [MESH:D009205] (1708) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Aortic Valve Insufficiency [MESH:D001022] (1002) |
|
|
|
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1451) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Thrombosis [MESH:D003328] (255) |
|
|
Coronary Vasospasm [MESH:D003329] (533) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Ventricular Dysfunction, Left [MESH:D018487] (1631) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Compartment Syndromes [MESH:D003161] (80) |
|
|
Hemorrhoids [MESH:D006484] (166) |
|
|
Hepatic Veno-Occlusive Disease [MESH:D006504] (208) |
|
|
Retinal Vein Occlusion [MESH:D012170] (607) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
|
|
|
Aortic Rupture [MESH:D001019] (637) |
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
Aortic Aneurysm, Thoracic [MESH:D017545] (781) |
|
|
Aortic Rupture [MESH:D001019] (637) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
Aortic Aneurysm, Thoracic [MESH:D017545] (781) |
|
|
Aortic Rupture [MESH:D001019] (637) |
|
|
Carotid Stenosis [MESH:D016893] (174) |
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Vertebrobasilar Insufficiency [MESH:D014715] (9) |
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
Vertebrobasilar Insufficiency [MESH:D014715] (9) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Carotid Artery Thrombosis [MESH:D002341] (138) |
|
|
Carotid Stenosis [MESH:D016893] (174) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Carotid Artery Thrombosis [MESH:D002341] (138) |
|
|
Sinus Thrombosis, Intracranial [MESH:D012851] (356) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
Hematoma, Subdural [MESH:D006408] (212) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
|
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Venous Thromboembolism [MESH:D054556] (400) |
|
|
Carotid Artery Thrombosis [MESH:D002341] (138) |
|
|
Sinus Thrombosis, Intracranial [MESH:D012851] (356) |
|
|
Coronary Thrombosis [MESH:D003328] (255) |
|
|
Venous Thromboembolism [MESH:D054556] (400) |
|
|
Carotid Artery Thrombosis [MESH:D002341] (138) |
|
|
Sinus Thrombosis, Intracranial [MESH:D012851] (356) |
|
|
Retinal Vein Occlusion [MESH:D012170] (607) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Hypertension, Essential [MESH:C562386] (1308) |
|
|
Hypotension, Orthostatic [MESH:D007024] (679) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Thrombosis [MESH:D003328] (255) |
|
|
Coronary Vasospasm [MESH:D003329] (533) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Spinal Cord Ischemia [MESH:D020760] (12) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
Methemoglobinemia [MESH:D008708] (850) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Thrombasthenia [MESH:D013915] (98) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
|
|
|
Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
|
|
Thrombasthenia [MESH:D013915] (98) |
|
|
Thrombocytopenia, Neonatal Alloimmune [MESH:D054098] (79) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
|
|
|
Hypoalbuminemia [MESH:D034141] (1332) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
|
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Thrombasthenia [MESH:D013915] (98) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Leukostasis [MESH:D018921] (769) |
|
|
|
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
|
|
Splenic Diseases [MESH:D013158] (1323) |
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Sarcoidosis [MESH:D012507] (895) |
|
|
Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) |
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
|
|
|
|
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
|
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
|
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Acromicric dysplasia [MESH:C535662] (520) |
|
|
Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Camurati-Engelmann Syndrome [MESH:D003966] (492) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Thrombasthenia [MESH:D013915] (98) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Myeloperoxidase Deficiency [MESH:C562864] (335) |
|
|
Coumarin Resistance [MESH:C563039] (397) |
|
|
Drug Metabolism, Poor, CYP2C19-Related [MESH:C563703] (182) |
|
|
Drug Metabolism, Poor, CYP2D6-Related [MESH:C563835] (220) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32) |
|
|
|
|
|
3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Li-Fraumeni Syndrome [MESH:D016864] (859) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Thrombocytopenia, Neonatal Alloimmune [MESH:D054098] (79) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Penile Induration [MESH:D010411] (495) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Keloid [MESH:D007627] (1111) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Exanthema [MESH:D005076] (301) |
|
|
Keratosis [MESH:D007642] (1941) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
Breast Neoplasms [MESH:D001943] (6077) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Drug Eruptions [MESH:D003875] (2697) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
|
|
|
|
|
Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Lichenoid Eruptions [MESH:D017512] (1324) |
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Angioedema [MESH:D000799] (837) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
|
|
|
3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Idiopathic basal ganglia calcification 1 [MESH:C536275] (139) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Li-Fraumeni Syndrome [MESH:D016864] (859) |
|
|
Hyperglycemia [MESH:D006943] (1858) |
|
|
Hypoglycemia [MESH:D007003] (2420) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
|
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
Myeloperoxidase Deficiency [MESH:C562864] (335) |
|
|
Coumarin Resistance [MESH:C563039] (397) |
|
|
Drug Metabolism, Poor, CYP2C19-Related [MESH:C563703] (182) |
|
|
Drug Metabolism, Poor, CYP2D6-Related [MESH:C563835] (220) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32) |
|
|
|
|
|
3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Mitochondrial Myopathies [MESH:D017240] (2176) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239) |
|
|
|
|
|
Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Obesity, Morbid [MESH:D009767] (515) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
|
|
|
|
|
|
|
|
Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Diabetic Neuropathies [MESH:D003929] (2443) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Pancreatic Neoplasms [MESH:D010190] (3820) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
|
|
|
|
|
|
Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Primary Ovarian Insufficiency [MESH:D016649] (270) |
|
|
|
|
|
Hyperparathyroidism, Secondary [MESH:D006962] (1138) |
|
|
Hyperthyroidism [MESH:D006980] (1191) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
|
|
|
Drug Eruptions [MESH:D003875] (2695) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Ige Responsiveness, Atopic [MESH:C564133] (267) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
Allergic Rhinitis [MESH:C567078] (181) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
|
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
|
|
|
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) |
|
|
|
|
|
|
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
 |
C22. Animal Diseases |
 |
 |
|
C22. Animal Diseases |
|
|
Mammary Neoplasms, Animal [MESH:D015674] (2735) |
|
|
Paratuberculosis [MESH:D010283] (427) |
|
|
Tuberculosis, Bovine [MESH:D014380] (380) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
Atrophy [MESH:D001284] (2603) |
|
|
Plaque, Atherosclerotic [MESH:D058226] (696) |
|
|
Ventricular Remodeling [MESH:D020257] (686) |
|
|
Hernia, Diaphragmatic [MESH:D006548] (2647) |
|
|
Intervertebral disc disease [MESH:C535531] (514) |
|
|
Cardiomegaly [MESH:D006332] (3802) |
|
|
Hepatomegaly [MESH:D006529] (1169) |
|
|
Splenomegaly [MESH:D013163] (1258) |
|
|
Emphysema [MESH:D004646] (1096) |
|
|
Gliosis [MESH:D005911] (1419) |
|
|
Growth Disorders [MESH:D006130] (2438) |
|
|
Hyperbilirubinemia [MESH:D006932] (1860) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Intraoperative Complications [MESH:D007431] (131) |
|
|
Ischemia [MESH:D007511] (3049) |
|
|
Metaplasia [MESH:D008679] (1469) |
|
|
Necrosis [MESH:D009336] (4019) |
|
|
Neointima [MESH:D058426] (814) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
|
|
|
Torsades de Pointes [MESH:D016171] (880) |
|
|
Translocation, Genetic [MESH:D014178] (557) |
|
|
|
|
|
|
|
|
Chromosome 17 deletion [MESH:C538045] (769) |
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Peritoneal Fibrosis [MESH:D056627] (488) |
|
|
Keloid [MESH:D007627] (1110) |
|
|
Postoperative Hemorrhage [MESH:D019106] (16) |
|
|
Shock, Hemorrhagic [MESH:D012771] (2042) |
|
|
Peptic Ulcer Hemorrhage [MESH:D010438] (553) |
|
|
Hematoma, Subdural [MESH:D006408] (215) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2872) |
|
|
Hematoma, Subdural [MESH:D006408] (212) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1081) |
|
|
|
|
|
Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
|
|
|
Shock, Septic [MESH:D012772] (1830) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
|
|
Neoplasm Metastasis [MESH:D009362] (4441) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
|
|
Pain, Postoperative [MESH:D010149] (529) |
|
|
Postoperative Hemorrhage [MESH:D019106] (16) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Multiple Organ Failure [MESH:D009102] (1836) |
|
|
Shock, Hemorrhagic [MESH:D012771] (2042) |
|
|
Shock, Septic [MESH:D012772] (1830) |
|
|
Edema [MESH:D004487] (3726) |
|
|
Fever [MESH:D005334] (2856) |
|
|
Hypothermia [MESH:D007035] (2075) |
|
|
Birth Weight [MESH:D001724] (377) |
|
|
Weight Gain [MESH:D015430] (2595) |
|
|
|
|
|
Cachexia [MESH:D002100] (2283) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Obesity, Morbid [MESH:D009767] (515) |
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Seizures [MESH:D012640] (4502) |
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Dystonia [MESH:D004421] (848) |
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Tremor [MESH:D014202] (840) |
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Coma [MESH:D003128] (492) |
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Syncope [MESH:D013575] (128) |
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Amnesia [MESH:D000647] (1911) |
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Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
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Hallucinations [MESH:D006212] (251) |
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Muscle Rigidity [MESH:D009127] (617) |
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Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
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Headache [MESH:D006261] (1417) |
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Neuralgia [MESH:D009437] (2074) |
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Deafness [MESH:D003638] (593) |
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Hyperalgesia [MESH:D006930] (3929) |
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Hypesthesia [MESH:D006987] (58) |
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Ageusia [MESH:D000370] (20) |
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Headache [MESH:D006261] (1417) |
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Neuralgia [MESH:D009437] (2074) |
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Pain, Postoperative [MESH:D010149] (529) |
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Acute Coronary Syndrome [MESH:D054058] (2286) |
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Angina, Stable [MESH:D060050] (1702) |
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Constipation [MESH:D003248] (506) |
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Nausea [MESH:D009325] (2300) |
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Vomiting [MESH:D014839] (1354) |
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Anoxia [MESH:D000860] (1698) |
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Dyspnea [MESH:D004417] (248) |
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Respiratory Sounds [MESH:D012135] (713) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222) |
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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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Not Fully Specified [NFS] (1530) |
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Agricultural Workers' Diseases [MESH:D000382] (193) |
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Persian Gulf Syndrome [MESH:D018923] (166) |
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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-Induced Liver Injury [MESH:D056486] (4936) |
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Drug Eruptions [MESH:D003875] (2697) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Lead Poisoning [MESH:D007855] (515) |
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Manganese Poisoning [MESH:D020149] (2214) |
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Neurotoxicity Syndromes [MESH:D020258] (3323) |
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Organophosphate Poisoning [MESH:D062025] (497) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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Marijuana Abuse [MESH:D002189] (1132) |
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Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Tobacco Use Disorder [MESH:D014029] (628) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Heroin Dependence [MESH:D006556] (950) |
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Morphine Dependence [MESH:D009021] (855) |
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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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Vascular System Injuries [MESH:D057772] (2086) |
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Brain Injuries [MESH:D001930] (3431) |
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Hematoma, Subdural [MESH:D006408] (212) |
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Hip Fractures [MESH:D006620] (81) |
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Hip Fractures [MESH:D006620] (82) |
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Hip Fractures [MESH:D006620] (81) |
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Hip Fractures [MESH:D006620] (82) |
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Radiation Injuries, Experimental [MESH:D011833] (2662) |
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Aortic Rupture [MESH:D001019] (637) |
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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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Hematoma, Subdural [MESH:D006408] (212) |
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D02. Organic Chemicals |
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D02. Organic Chemicals |
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Ticlopidine [MESH:D013988] (8) |
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D03. Heterocyclic Compounds |
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D03. Heterocyclic Compounds |
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Ticlopidine [MESH:D013988] (8) |
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Ticlopidine [MESH:D013988] (8) |
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Ticlopidine [MESH:D013988] (8) |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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F. Psychiatry and Psychology |
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F. Psychiatry and Psychology |
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Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
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Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
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G. Phenomena and Processes |
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G. Phenomena and Processes |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
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|
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Chromosome 17 deletion [MESH:C538045] (769) |
|
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|
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Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Chromosome 17 deletion [MESH:C538045] (769) |
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
|
|
|
|
|
|
|
|
|
Chromosome 17 deletion [MESH:C538045] (769) |
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
|
|
|
Chromosome 17 deletion [MESH:C538045] (769) |
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
|
|
|
|
|
|
|
|
|
Chromosome 17 deletion [MESH:C538045] (769) |
|
|
Hypotonia-Cystinuria Syndrome [MESH:C564710] (52) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
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|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
 |