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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nuclear factor, erythroid 2-like 2 [HGNC:NFE2L2] (213) |
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kelch-like ECH-associated protein 1 [HGNC:KEAP1] (50) |
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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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glutathione S-transferase alpha 1 [HGNC:GSTA1] (114) |
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glutathione S-transferase alpha 2 [HGNC:GSTA2] (44) |
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glutathione S-transferase mu 3 (brain) [HGNC:GSTM3] (41) |
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glutathione S-transferase pi 1 [HGNC:GSTP1] (218) |
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glutathione S-transferase theta 1 [HGNC:GSTT1] (81) |
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glutathione S-transferase zeta 1 [HGNC:GSTZ1] (31) |
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heat shock 27kDa protein 01 [HGNC:HSPB1] (84) |
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kelch-like ECH-associated protein 1 [HGNC:KEAP1] (50) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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cotreatment (1499) |
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metabolic processing (485) |
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oxidation (19) |
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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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abundance (630) |
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activity (2865) |
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expression (3238) |
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metabolic processing (740) |
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oxidation (295) |
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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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Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
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Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
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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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Mycoplasma Infections [MESH:D009175] (1947) |
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Listeriosis [MESH:D008088] (1622) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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Urinary Tract Infections [MESH:D014552] (984) |
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Shock, Septic [MESH:D012772] (1830) |
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Endotoxemia [MESH:D019446] (1289) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Endotoxemia [MESH:D019446] (1289) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Hepatitis C [MESH:D006526] (1627) |
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Hepatitis C [MESH:D006526] (1627) |
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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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Trichuriasis [MESH:D014257] (805) |
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Schistosomiasis mansoni [MESH:D012555] (1033) |
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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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Neoplasms, Second Primary [MESH:D016609] (518) |
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Hamartoma Syndrome, Multiple [MESH:D006223] (262) |
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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, Myeloid, Acute [MESH:D015470] (2176) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Carcinosarcoma [MESH:D002296] (581) |
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Chondroma [MESH:D002812] (155) |
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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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Carcinosarcoma [MESH:D002296] (581) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Osteosarcoma [MESH:D012516] (2175) |
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Testicular Germ Cell Tumor [MESH:C563236] (176) |
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Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) |
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Gliosarcoma [MESH:D018316] (880) |
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Oligodendroglioma [MESH:D009837] (241) |
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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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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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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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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Mesothelioma [MESH:D008654] (2567) |
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Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) |
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Gliosarcoma [MESH:D018316] (880) |
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Oligodendroglioma [MESH:D009837] (241) |
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Glioblastoma [MESH:D005909] (2554) |
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Papilloma [MESH:D010212] (2243) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) |
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Gliosarcoma [MESH:D018316] (880) |
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Oligodendroglioma [MESH:D009837] (241) |
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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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Hemangioma [MESH:D006391] (690) |
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Melanoma [MESH:D008545] (3508) |
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Bone Neoplasms [MESH:D001859] (1334) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Soft Tissue Neoplasms [MESH:D012983] (2003) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Gallbladder Neoplasms [MESH:D005706] (993) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Testicular Germ Cell Tumor [MESH:C563236] (176) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Brain Neoplasms [MESH:D001932] (2764) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Endometrial Neoplasms [MESH:D016889] (1987) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Testicular Germ Cell Tumor [MESH:C563236] (176) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Hamartoma Syndrome, Multiple [MESH:D006223] (262) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Hamartoma Syndrome, Multiple [MESH:D006223] (260) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Bone Neoplasms [MESH:D001859] (1334) |
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Acromicric dysplasia [MESH:C535662] (520) |
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Craniofacial Dysostosis [MESH:D003394] (391) |
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Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
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Jackson-Weiss syndrome [MESH:C537559] (149) |
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Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
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Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
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Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
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Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
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Camurati-Engelmann Syndrome [MESH:D003966] (492) |
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Enchondromatosis [MESH:D004687] (170) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Osteolysis [MESH:D010014] (1787) |
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Intervertebral Disc Degeneration [MESH:D055959] (827) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Jackson-Weiss syndrome [MESH:C537559] (149) |
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Cleft Palate [MESH:D002972] (1330) |
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Ankylosis [MESH:D000844] (479) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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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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Rhabdomyolysis [MESH:D012206] (465) |
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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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Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
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Dermatomyositis [MESH:D003882] (1826) |
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Dermatomyositis [MESH:D003882] (1826) |
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Craniofacial Dysostosis [MESH:D003394] (391) |
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Jackson-Weiss syndrome [MESH:C537559] (149) |
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Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
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Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
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Cleft Palate [MESH:D002972] (1330) |
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
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Plagiocephaly, Nonsynostotic [MESH:D049068] (85) |
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Jackson-Weiss syndrome [MESH:C537559] (149) |
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Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
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Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
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Acromicric dysplasia [MESH:C535662] (520) |
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Jackson-Weiss syndrome [MESH:C537559] (149) |
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Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
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Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
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Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
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Jackson-Weiss syndrome [MESH:C537559] (149) |
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Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
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Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
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Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
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Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
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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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Gallbladder Neoplasms [MESH:D005706] (993) |
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Gallbladder Neoplasms [MESH:D005706] (993) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Gallbladder Neoplasms [MESH:D005706] (993) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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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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Barrett Esophagus [MESH:D001471] (1930) |
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Gastroesophageal Reflux [MESH:D005764] (1465) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Mucositis [MESH:D052016] (1238) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Enterocolitis, Necrotizing [MESH:D020345] (1367) |
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Gastritis, Atrophic [MESH:D005757] (947) |
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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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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Enterocolitis, Necrotizing [MESH:D020345] (1367) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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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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Gastritis, Atrophic [MESH:D005757] (947) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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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, 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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Cystic Fibrosis [MESH:D003550] (760) |
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Pancreatitis [MESH:D010195] (1924) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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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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Cleft Palate [MESH:D002972] (1330) |
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (98) |
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Behcet Syndrome [MESH:D001528] (1784) |
|
|
Mucositis [MESH:D052016] (1238) |
|
|
Oral Submucous Fibrosis [MESH:D009914] (2432) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Tongue Neoplasms [MESH:D014062] (1518) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Tongue Neoplasms [MESH:D014062] (1518) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (98) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
|
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
 |
C08. Respiratory Tract Diseases |
 |
 |
|
C08. Respiratory Tract Diseases |
|
|
Not Fully Specified [NFS] (1984) |
|
|
|
|
|
Bronchiectasis [MESH:D001987] (1792) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Pulmonary Edema [MESH:D011654] (2109) |
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Pulmonary Fibrosis [MESH:D011658] (3140) |
|
|
|
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Silicosis [MESH:D012829] (1273) |
|
|
Asthma [MESH:D001249] (3903) |
|
|
Pulmonary Emphysema [MESH:D011656] (1259) |
|
|
Acute Lung Injury [MESH:D055371] (1907) |
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Silicosis [MESH:D012829] (1273) |
|
|
Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
|
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
|
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
 |
C09. Otorhinolaryngologic Diseases |
 |
 |
|
C09. Otorhinolaryngologic Diseases |
|
|
|
|
|
|
|
|
|
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
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 Edema [MESH:D001929] (1165) |
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
Brain Neoplasms [MESH:D001932] (2764) |
|
|
|
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Brain Ischemia [MESH:D002545] (4873) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
Stroke [MESH:D020521] (3702) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
|
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
|
|
|
Migraine Disorders [MESH:D008881] (2318) |
|
|
|
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
|
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
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) |
|
|
Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219) |
|
|
|
|
|
|
|
|
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) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
Brain Neoplasms [MESH:D001932] (2764) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239) |
|
|
Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219) |
|
|
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) |
|
|
Lethargy [MESH:D053609] (1035) |
|
|
Memory Disorders [MESH:D008569] (3233) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Neuralgia [MESH:D009437] (2074) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
|
|
|
|
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239) |
|
|
Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219) |
|
|
Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219) |
|
|
|
|
|
|
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Diabetic Neuropathies [MESH:D003929] (2442) |
|
|
Neuralgia [MESH:D009437] (2078) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
|
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
Dry Eye Syndromes [MESH:D015352] (533) |
|
|
|
|
|
Glaucoma, Open-Angle [MESH:D005902] (1281) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
|
|
|
|
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Testicular Germ Cell Tumor [MESH:C563236] (176) |
|
|
|
|
|
Asthenozoospermia [MESH:D053627] (298) |
|
|
Penile Induration [MESH:D010411] (495) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Testicular Germ Cell Tumor [MESH:C563236] (176) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
 |
C13. Female Urogenital Diseases and Pregnancy Complications |
 |
 |
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
|
|
|
|
|
|
|
|
|
Primary Ovarian Insufficiency [MESH:D016649] (270) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
|
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
Placenta Diseases [MESH:D010922] (1781) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Embryo Loss [MESH:D020964] (288) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Cardiovascular Abnormalities [MESH:D018376] (3153) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Pericardial Effusion [MESH:D010490] (1015) |
|
|
Ventricular Dysfunction [MESH:D018754] (2348) |
|
|
|
|
|
|
|
|
Torsades de Pointes [MESH:D016171] (880) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1516) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocarditis [MESH:D009205] (1708) |
|
|
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 Vasospasm [MESH:D003329] (533) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Hemorrhoids [MESH:D006484] (166) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
|
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Brain Ischemia [MESH:D002545] (4873) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
Stroke [MESH:D020521] (3702) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Thrombosis [MESH:D013927] (3101) |
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Hypertension, Essential [MESH:C562386] (1308) |
|
|
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 Vasospasm [MESH:D003329] (533) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Raynaud Disease [MESH:D011928] (490) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
|
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Favism [MESH:D005236] (193) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Favism [MESH:D005236] (193) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
|
|
|
|
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134) |
|
|
Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Leukocytosis [MESH:D007964] (988) |
|
|
Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
Granulomatous Disease, Chronic [MESH:D006105] (404) |
|
|
|
|
|
Sarcoidosis [MESH:D012507] (895) |
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
|
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
Abnormalities, Drug-Induced [MESH:D000014] (1024) |
|
|
Cardiovascular Abnormalities [MESH:D018376] (3294) |
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
|
|
|
Craniofacial Dysostosis [MESH:D003394] (391) |
|
|
Jackson-Weiss syndrome [MESH:C537559] (149) |
|
|
Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
|
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
|
|
Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Plagiocephaly, Nonsynostotic [MESH:D049068] (85) |
|
|
Jackson-Weiss syndrome [MESH:C537559] (149) |
|
|
Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
|
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
|
|
Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
|
|
Acromicric dysplasia [MESH:C535662] (520) |
|
|
Jackson-Weiss syndrome [MESH:C537559] (149) |
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
|
|
Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
|
|
Jackson-Weiss syndrome [MESH:C537559] (149) |
|
|
Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
|
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
|
|
Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
Camurati-Engelmann Syndrome [MESH:D003966] (492) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Favism [MESH:D005236] (193) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Granulomatous Disease, Chronic [MESH:D006105] (404) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Myeloperoxidase Deficiency [MESH:C562864] (335) |
|
|
Coumarin Resistance [MESH:C563039] (397) |
|
|
Drug Metabolism, Poor, CYP2C19-Related [MESH:C563703] (182) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (195) |
|
|
Mucopolysaccharidosis VII [MESH:D016538] (88) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
|
|
|
Mucopolysaccharidosis VII [MESH:D016538] (88) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Acatalasia [MESH:D020642] (788) |
|
|
Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Hamartoma Syndrome, Multiple [MESH:D006223] (260) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Asphyxia Neonatorum [MESH:D001238] (1648) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
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) |
|
|
Penile Induration [MESH:D010411] (495) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Keloid [MESH:D007627] (1111) |
|
|
|
|
|
Mucopolysaccharidosis VII [MESH:D016538] (88) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Keratosis [MESH:D007642] (1941) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
|
|
|
|
|
|
Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
|
|
Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
|
|
Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
|
|
|
|
|
|
Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
|
|
|
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
|
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
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) |
|
|
|
|
|
|
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
Myeloperoxidase Deficiency [MESH:C562864] (335) |
|
|
Coumarin Resistance [MESH:C563039] (397) |
|
|
Drug Metabolism, Poor, CYP2C19-Related [MESH:C563703] (182) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (195) |
|
|
Mucopolysaccharidosis VII [MESH:D016538] (88) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
|
|
|
Mucopolysaccharidosis VII [MESH:D016538] (88) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Acatalasia [MESH:D020642] (788) |
|
|
Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
|
|
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) |
|
|
Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
|
|
|
|
|
|
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 |
|
|
|
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
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) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Testicular Germ Cell Tumor [MESH:C563236] (176) |
|
|
Puberty, Precocious [MESH:D011629] (1147) |
|
|
Primary Ovarian Insufficiency [MESH:D016649] (270) |
|
|
|
|
|
Testicular Germ Cell Tumor [MESH:C563236] (176) |
|
|
Hyperthyroidism [MESH:D006980] (1191) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
|
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Granulomatous Disease, Chronic [MESH:D006105] (404) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
|
|
|
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) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
Ventricular Remodeling [MESH:D020257] (686) |
|
|
Hernia, Diaphragmatic [MESH:D006548] (2647) |
|
|
Cardiomegaly [MESH:D006332] (3802) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Intestinal Polyps [MESH:D007417] (1592) |
|
|
Emphysema [MESH:D004646] (1096) |
|
|
Hemolysis [MESH:D006461] (280) |
|
|
Hyperbilirubinemia [MESH:D006932] (1860) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Leukocytosis [MESH:D007964] (978) |
|
|
Necrosis [MESH:D009336] (4019) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
|
|
|
|
|
|
Torsades de Pointes [MESH:D016171] (880) |
|
|
Micronuclei, Chromosome-Defective [MESH:D048629] (1013) |
|
|
Embryo Loss [MESH:D020964] (288) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Disease Susceptibility [MESH:D004198] (1200) |
|
|
Recurrence [MESH:D012008] (830) |
|
|
Peritoneal Fibrosis [MESH:D056627] (488) |
|
|
Keloid [MESH:D007627] (1110) |
|
|
Shock, Hemorrhagic [MESH:D012771] (2042) |
|
|
Peptic Ulcer Hemorrhage [MESH:D010438] (553) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1081) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
|
|
|
Shock, Septic [MESH:D012772] (1830) |
|
|
Endotoxemia [MESH:D019446] (1289) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
|
|
Neoplasm Metastasis [MESH:D009362] (4441) |
|
|
Neoplasm Recurrence, Local [MESH:D009364] (1949) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
|
|
|
|
|
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) |
|
|
Obesity [MESH:D009765] (4454) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Sleep Disorders [MESH:D012893] (1301) |
|
|
Lethargy [MESH:D053609] (1035) |
|
|
Memory Disorders [MESH:D008569] (3233) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
|
|
Neuralgia [MESH:D009437] (2074) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
|
|
|
|
|
|
Lacrimoauriculodentodigital syndrome [MESH:C538132] (149) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
Neuralgia [MESH:D009437] (2074) |
|
|
|
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Constipation [MESH:D003248] (506) |
|
|
Nausea [MESH:D009325] (2300) |
|
|
Anoxia [MESH:D000860] (1698) |
|
|
Respiratory Sounds [MESH:D012135] (713) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
 |
C24. Occupational Diseases |
 |
 |
|
C24. Occupational Diseases |
|
|
Not Fully Specified [NFS] (1530) |
|
|
Agricultural Workers' Diseases [MESH:D000382] (193) |
|
|
Persian Gulf Syndrome [MESH:D018923] (166) |
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Silicosis [MESH:D012829] (1273) |
|
 |
C25. Chemically-Induced Disorders |
 |
 |
|
C25. Chemically-Induced Disorders |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Cadmium Poisoning [MESH:D002105] (180) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
Organophosphate Poisoning [MESH:D062025] (497) |
|
|
Psychoses, Substance-Induced [MESH:D011605] (2053) |
|
|
Favism [MESH:D005236] (193) |
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Favism [MESH:D005236] (193) |
|
|
Amphetamine-Related Disorders [MESH:D019969] (2858) |
|
|
Psychoses, Substance-Induced [MESH:D011605] (2052) |
|
|
Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Alcoholism [MESH:D000437] (1519) |
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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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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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Brain Injuries [MESH:D001930] (3431) |
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D02. Organic Chemicals |
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D02. Organic Chemicals |
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Benzene Derivatives [MESH:D001555] (10684) |
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F. Psychiatry and Psychology |
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F. Psychiatry and Psychology |
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
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Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) |
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