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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nuclear factor, erythroid 2-like 2 [HGNC:NFE2L2] (213) |
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ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355) |
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cytochrome P450, family 02, subfamily B, polypeptide 06 [HGNC:CYP2B6] (216) |
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cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612) |
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estrogen receptor 1 [HGNC:ESR1] (506) |
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nuclear receptor subfamily 1, group I, member 2 [HGNC:NR1I2] (328) |
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progesterone receptor [HGNC:PGR] (209) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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binding (2423) |
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cotreatment (1499) |
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reaction (624) |
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reaction (3393) |
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response to substance (713) |
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activity (2865) |
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expression (3238) |
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metabolic processing (740) |
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response to substance (641) |
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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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Aortic Valve, Calcification of [MESH:C562942] (655) |
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Heinz Body Anemias [MESH:C563030] (127) |
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Heinz Body Anemias [MESH:C563030] (127) |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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Heinz Body Anemias [MESH:C563030] (127) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Helicobacter Infections [MESH:D016481] (579) |
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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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Tuberculosis, Pulmonary [MESH:D014397] (678) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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Urinary Tract Infections [MESH:D014552] (984) |
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Peritonitis [MESH:D010538] (800) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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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 B [MESH:D006509] (976) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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WHIM syndrome [MESH:C536697] (148) |
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Hepatitis B [MESH:D006509] (976) |
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Hepatitis C [MESH:D006526] (1627) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Arenaviridae Infections [MESH:D001117] (204) |
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Hepatitis C [MESH:D006526] (1627) |
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Influenza, Human [MESH:D007251] (1075) |
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Cardiovirus Infections [MESH:D018188] (1548) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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WHIM syndrome [MESH:C536697] (148) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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WHIM syndrome [MESH:C536697] (148) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Schistosomiasis mansoni [MESH:D012555] (1033) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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Malaria, Falciparum [MESH:D016778] (438) |
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Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
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C04. Neoplasms |
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C04. Neoplasms |
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Hamartoma [MESH:D006222] (1484) |
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Precancerous Conditions [MESH:D011230] (2858) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Lymphoma, Follicular [MESH:D008224] (1025) |
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Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420) |
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Lymphoma, Mantle-Cell [MESH:D020522] (561) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420) |
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Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
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Sarcoma, Synovial [MESH:D013584] (993) |
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Chondrosarcoma, Mesenchymal [MESH:D018211] (1161) |
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Mastocytosis, Systemic [MESH:D034721] (769) |
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Osteosarcoma [MESH:D012516] (2175) |
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Fibromatosis, Aggressive [MESH:D018222] (1562) |
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Leiomyoma [MESH:D007889] (744) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Osteosarcoma [MESH:D012516] (2175) |
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Sarcoma, Synovial [MESH:D013584] (993) |
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Chondrosarcoma, Mesenchymal [MESH:D018211] (1161) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Gliosarcoma [MESH:D018316] (880) |
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Medulloblastoma [MESH:D008527] (1282) |
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Glioblastoma [MESH:D005909] (2554) |
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Medulloblastoma [MESH:D008527] (1282) |
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Neuroblastoma [MESH:D009447] (1420) |
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Melanoma, Amelanotic [MESH:D018328] (65) |
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Melanoma, Experimental [MESH:D008546] (210) |
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Adenoma, Liver Cell [MESH:D018248] (685) |
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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, 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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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Mesothelioma [MESH:D008654] (2567) |
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Gliosarcoma [MESH:D018316] (880) |
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Medulloblastoma [MESH:D008527] (1282) |
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Glioblastoma [MESH:D005909] (2554) |
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Medulloblastoma [MESH:D008527] (1282) |
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Neuroblastoma [MESH:D009447] (1420) |
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Papilloma [MESH:D010212] (2243) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Meningioma [MESH:D008579] (978) |
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Gliosarcoma [MESH:D018316] (880) |
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Medulloblastoma [MESH:D008527] (1282) |
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Glioblastoma [MESH:D005909] (2554) |
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Medulloblastoma [MESH:D008527] (1282) |
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Neuroblastoma [MESH:D009447] (1420) |
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Melanoma, Amelanotic [MESH:D018328] (65) |
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Melanoma, Experimental [MESH:D008546] (210) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Meningioma [MESH:D008579] (978) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Melanoma, Amelanotic [MESH:D018328] (65) |
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Melanoma, Experimental [MESH:D008546] (210) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Soft Tissue Neoplasms [MESH:D012983] (2003) |
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Nose Neoplasms [MESH:D009669] (384) |
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Breast Neoplasms, Male [MESH:D018567] (650) |
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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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Cecal Neoplasms [MESH:D002430] (822) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Anus Neoplasms [MESH:D001005] (69) |
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Adenoma, Liver Cell [MESH:D018248] (685) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Laryngeal Neoplasms [MESH:D007822] (68) |
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Nose Neoplasms [MESH:D009669] (390) |
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Nasopharyngeal carcinoma [MESH:C538339] (1198) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Brain Neoplasms [MESH:D001932] (2764) |
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Meningioma [MESH:D008579] (978) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Small Cell Lung Carcinoma [MESH:D055752] (1380) |
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Endometrial Neoplasms [MESH:D016889] (1987) |
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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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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Melanoma, Experimental [MESH:D008546] (210) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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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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Peutz-Jeghers Syndrome [MESH:D010580] (51) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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WHIM syndrome [MESH:C536697] (148) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Osteonecrosis [MESH:D010020] (539) |
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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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Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
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Marshall syndrome [MESH:C536025] (52) |
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Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
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Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
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Congenital disorder of glycosylation type 2A [MESH:C535752] (38) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
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Nose Neoplasms [MESH:D009669] (384) |
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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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Mandibular Diseases [MESH:D008336] (395) |
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Maxillary Diseases [MESH:D008439] (354) |
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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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Erythrocyte Lactate Transporter Defect [MESH:C565449] (106) |
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Mitochondrial Myopathies [MESH:D017240] (2176) |
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Myopathies, Structural, Congenital [MESH:D020914] (272) |
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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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Marshall syndrome [MESH:C536025] (52) |
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Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
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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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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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Cecal Neoplasms [MESH:D002430] (822) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Anus Neoplasms [MESH:D001005] (69) |
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Adenoma, Liver Cell [MESH:D018248] (685) |
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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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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Enterocolitis, Necrotizing [MESH:D020345] (1367) |
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Inflammatory Bowel Disease 13 [MESH:C567384] (435) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Anus Neoplasms [MESH:D001005] (69) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Enterocolitis, Necrotizing [MESH:D020345] (1367) |
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Inflammatory Bowel Disease 13 [MESH:C567384] (435) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Anus Neoplasms [MESH:D001005] (69) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Peutz-Jeghers Syndrome [MESH:D010580] (51) |
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Lactose Intolerance, Adult Type [MESH:C562601] (112) |
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Anus Neoplasms [MESH:D001005] (69) |
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Anus Neoplasms [MESH:D001005] (69) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Gastroparesis [MESH:D018589] (732) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Stomach Ulcer [MESH:D013276] (2915) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Fatty Liver [MESH:D005234] (3584) |
|
|
Hepatomegaly [MESH:D006529] (1169) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
|
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
Liver Failure, Acute [MESH:D017114] (2404) |
|
|
Hepatitis, Alcoholic [MESH:D006519] (1613) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Hepatitis B [MESH:D006509] (976) |
|
|
Hepatitis C [MESH:D006526] (1627) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
|
|
Hepatitis, Alcoholic [MESH:D006519] (1613) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Adenoma, Liver Cell [MESH:D018248] (685) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Peritonitis [MESH:D010538] (800) |
|
 |
C07. Stomatognathic Diseases |
 |
 |
|
C07. Stomatognathic Diseases |
|
|
|
|
|
Mandibular Diseases [MESH:D008336] (450) |
|
|
Maxillary Diseases [MESH:D008439] (354) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Oral Submucous Fibrosis [MESH:D009914] (2432) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
Periodontitis [MESH:D010518] (843) |
|
|
Salivary Gland Neoplasms [MESH:D012468] (968) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
 |
C08. Respiratory Tract Diseases |
 |
 |
|
C08. Respiratory Tract Diseases |
|
|
Not Fully Specified [NFS] (1984) |
|
|
|
|
|
Asthma [MESH:D001249] (4098) |
|
|
Bronchial Hyperreactivity [MESH:D016535] (1357) |
|
|
Bronchiectasis [MESH:D001987] (1792) |
|
|
Laryngeal Neoplasms [MESH:D007822] (68) |
|
|
Hypertension, Pulmonary [MESH:D006976] (2000) |
|
|
Pulmonary Edema [MESH:D011654] (2109) |
|
|
Pulmonary Fibrosis [MESH:D011658] (3140) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
|
|
|
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) |
|
|
|
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Silicosis [MESH:D012829] (1273) |
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
Nose Neoplasms [MESH:D009669] (390) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Asthma [MESH:D001249] (4098) |
|
|
Influenza, Human [MESH:D007251] (1075) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
Laryngeal Neoplasms [MESH:D007822] (68) |
|
|
Nose Neoplasms [MESH:D009669] (390) |
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
 |
C09. Otorhinolaryngologic Diseases |
 |
 |
|
C09. Otorhinolaryngologic Diseases |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Marshall syndrome [MESH:C536025] (52) |
|
|
Laryngeal Neoplasms [MESH:D007822] (68) |
|
|
Nose Neoplasms [MESH:D009669] (390) |
|
|
Laryngeal Neoplasms [MESH:D007822] (68) |
|
|
Nose Neoplasms [MESH:D009669] (390) |
|
|
|
|
|
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) |
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
|
|
|
|
|
|
Hypotension, Orthostatic [MESH:D007024] (679) |
|
|
|
|
|
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) |
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Pelizaeus-Merzbacher Disease [MESH:D020371] (103) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
|
|
|
|
|
|
Migraine without Aura [MESH:D020326] (408) |
|
|
|
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Pelizaeus-Merzbacher Disease [MESH:D020371] (103) |
|
|
|
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Spinal Cord Compression [MESH:D013117] (1800) |
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
|
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Pelizaeus-Merzbacher Disease [MESH:D020371] (103) |
|
|
|
|
|
|
|
|
Spastic paraplegia 2, X-linked [MESH:C536857] (37) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
Brain Neoplasms [MESH:D001932] (2764) |
|
|
Meningioma [MESH:D008579] (978) |
|
|
von Hippel-Lindau Disease [MESH:D006623] (580) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
|
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
|
|
|
Spastic paraplegia 2, X-linked [MESH:C536857] (37) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Catalepsy [MESH:D002375] (1429) |
|
|
Hyperkinesis [MESH:D006948] (1799) |
|
|
Hypokinesia [MESH:D018476] (279) |
|
|
Memory Disorders [MESH:D008569] (3233) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Prader-Willi Syndrome [MESH:D011218] (46) |
|
|
Williams Syndrome [MESH:D018980] (133) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
Neuralgia [MESH:D009437] (2074) |
|
|
|
|
|
|
|
|
|
|
|
Marshall syndrome [MESH:C536025] (52) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
Erythrocyte Lactate Transporter Defect [MESH:C565449] (106) |
|
|
Mitochondrial Myopathies [MESH:D017240] (2176) |
|
|
Myopathies, Structural, Congenital [MESH:D020914] (272) |
|
|
|
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Diabetic Neuropathies [MESH:D003929] (2442) |
|
|
Neuralgia [MESH:D009437] (2078) |
|
|
Sciatic Neuropathy [MESH:D020426] (477) |
|
|
|
|
|
|
|
|
Spastic paraplegia 2, X-linked [MESH:C536857] (37) |
|
|
|
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
|
|
|
|
|
|
Marshall syndrome [MESH:C536025] (52) |
|
|
|
|
|
Glaucoma, Angle-Closure [MESH:D015812] (73) |
|
|
Retinal Degeneration [MESH:D012162] (2386) |
|
|
|
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Stickler syndrome, type 2 [MESH:C537493] (52) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Azoospermia [MESH:D053713] (1052) |
|
|
Oligospermia [MESH:D009845] (799) |
|
|
|
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Erectile Dysfunction [MESH:D007172] (1791) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
|
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
 |
C13. Female Urogenital Diseases and Pregnancy Complications |
 |
 |
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
Not Fully Specified [NFS] (1116) |
|
|
|
|
|
Endometriosis [MESH:D004715] (2461) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
|
|
|
|
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
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) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Diabetes, Gestational [MESH:D016640] (1157) |
|
|
Placenta Diseases [MESH:D010922] (1781) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Prenatal Injuries [MESH:D049188] (1314) |
|
|
Pre-Eclampsia [MESH:D011225] (1435) |
|
|
Fetal Membranes, Premature Rupture [MESH:D005322] (356) |
|
|
Obstetric Labor, Premature [MESH:D007752] (1316) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
|
|
|
Coronary Vessel Anomalies [MESH:D003330] (317) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Ventricular Dysfunction [MESH:D018754] (2348) |
|
|
|
|
|
|
|
|
Torsades de Pointes [MESH:D016171] (880) |
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1516) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocarditis [MESH:D009205] (1708) |
|
|
Coronary Vessel Anomalies [MESH:D003330] (317) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Aortic Valve Insufficiency [MESH:D001022] (1002) |
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1451) |
|
|
Williams Syndrome [MESH:D018980] (133) |
|
|
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 Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
|
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Aortic Stenosis, Supravalvular [MESH:D021921] (50) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Diabetic Angiopathies [MESH:D003925] (1984) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Peripheral Vascular Diseases [MESH:D016491] (1412) |
|
|
Varicose Veins [MESH:D014648] (383) |
|
|
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) |
|
|
von Hippel-Lindau Disease [MESH:D006623] (580) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
Aortic Aneurysm, Thoracic [MESH:D017545] (781) |
|
|
Aortic Rupture [MESH:D001019] (637) |
|
|
|
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Thrombosis [MESH:D013927] (3101) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos syndrome type 2 [MESH:C536195] (55) |
|
|
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 Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
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 |
|
|
Blood Coagulation Disorders [MESH:D001778] (1828) |
|
|
Methemoglobinemia [MESH:D008708] (850) |
|
|
Polycythemia [MESH:D011086] (412) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to [MESH:C565557] (312) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Heinz Body Anemias [MESH:C563030] (127) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
alpha-Thalassemia [MESH:D017085] (176) |
|
|
beta-Thalassemia [MESH:D017086] (458) |
|
|
Anemia, Iron-Deficiency [MESH:D018798] (547) |
|
|
|
|
|
|
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
Polycythemia Vera [MESH:D011087] (244) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
alpha-Thalassemia [MESH:D017085] (192) |
|
|
beta-Thalassemia [MESH:D017086] (458) |
|
|
Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos syndrome type 2 [MESH:C536195] (55) |
|
|
|
|
|
|
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
Splenic Diseases [MESH:D013158] (1323) |
|
|
|
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
Burkitt Lymphoma [MESH:D002051] (691) |
|
|
Lymphoma, Follicular [MESH:D008224] (1025) |
|
|
Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420) |
|
|
Lymphoma, Mantle-Cell [MESH:D020522] (561) |
|
|
Burkitt Lymphoma [MESH:D002051] (691) |
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
|
Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
|
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Prader-Willi Syndrome [MESH:D011218] (46) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
|
|
|
Coronary Vessel Anomalies [MESH:D003330] (317) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Prader-Willi Syndrome [MESH:D011218] (46) |
|
|
Williams Syndrome [MESH:D018980] (133) |
|
|
|
|
|
Marshall syndrome [MESH:C536025] (52) |
|
|
Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
|
|
|
|
|
|
|
|
Spastic paraplegia 2, X-linked [MESH:C536857] (37) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos syndrome type 2 [MESH:C536195] (55) |
|
|
|
|
|
|
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Heinz Body Anemias [MESH:C563030] (127) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
alpha-Thalassemia [MESH:D017085] (176) |
|
|
beta-Thalassemia [MESH:D017086] (458) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Prader-Willi Syndrome [MESH:D011218] (46) |
|
|
Williams Syndrome [MESH:D018980] (133) |
|
|
|
|
|
Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
|
|
Spastic paraplegia 2, X-linked [MESH:C536857] (37) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Pelizaeus-Merzbacher Disease [MESH:D020371] (103) |
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
alpha-Thalassemia [MESH:D017085] (192) |
|
|
beta-Thalassemia [MESH:D017086] (458) |
|
|
|
|
|
|
|
|
Spastic paraplegia 2, X-linked [MESH:C536857] (37) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Pelizaeus-Merzbacher Disease [MESH:D020371] (103) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Hyperglycerolemia [MESH:C538138] (46) |
|
|
Congenital disorder of glycosylation type 2A [MESH:C535752] (38) |
|
|
Lactose Intolerance, Adult Type [MESH:C562601] (112) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Peutz-Jeghers Syndrome [MESH:D010580] (51) |
|
|
Cutis Laxa [MESH:D003483] (177) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos syndrome type 2 [MESH:C536195] (55) |
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
Stickler syndrome, type 2 [MESH:C537493] (52) |
|
|
Cutis Laxa [MESH:D003483] (177) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Keloid [MESH:D007627] (1111) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos syndrome type 2 [MESH:C536195] (55) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
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) |
|
|
|
|
|
Breast Neoplasms, Male [MESH:D018567] (650) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Occupational [MESH:D009783] (311) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Alopecia [MESH:D000505] (1453) |
|
|
|
|
|
|
|
|
|
|
|
Peutz-Jeghers Syndrome [MESH:D010580] (51) |
|
|
|
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos syndrome type 2 [MESH:C536195] (55) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Occupational [MESH:D009783] (311) |
|
|
Cutis Laxa [MESH:D003483] (177) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
|
|
Ehlers-Danlos syndrome type 2 [MESH:C536195] (55) |
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
|
|
|
|
|
WHIM syndrome [MESH:C536697] (148) |
|
|
|
|
|
Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
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) |
|
|
|
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Pelizaeus-Merzbacher Disease [MESH:D020371] (103) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
|
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hyperglycemia [MESH:D006943] (1858) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106) |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106) |
|
|
Anemia, Iron-Deficiency [MESH:D018798] (547) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
Lactose Intolerance, Adult Type [MESH:C562601] (112) |
|
|
|
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Pelizaeus-Merzbacher Disease [MESH:D020371] (103) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Hyperglycerolemia [MESH:C538138] (46) |
|
|
Congenital disorder of glycosylation type 2A [MESH:C535752] (38) |
|
|
Lactose Intolerance, Adult Type [MESH:C562601] (112) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
Mitochondrial Myopathies [MESH:D017240] (2176) |
|
|
|
|
|
|
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
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) |
|
|
|
|
|
|
|
|
Familial Hypophosphatemic Rickets [MESH:D053098] (274) |
|
|
|
|
|
Prader-Willi Syndrome [MESH:D011218] (46) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetic Angiopathies [MESH:D003925] (1984) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Diabetic Neuropathies [MESH:D003929] (2443) |
|
|
|
|
|
Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
|
|
|
|
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
Hyperparathyroidism [MESH:D006961] (1475) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
|
|
|
Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
|
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
|
|
|
|
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Asthma [MESH:D001249] (3914) |
|
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WHIM syndrome [MESH:C536697] (148) |
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Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Lymphoma, Follicular [MESH:D008224] (1025) |
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Lymphoma, Mantle-Cell [MESH:D020522] (561) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420) |
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Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
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Multiple Myeloma [MESH:D009101] (2765) |
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C22. Animal Diseases |
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C22. Animal Diseases |
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Disease Models, Animal [MESH:D004195] (2058) |
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Mammary Neoplasms, Animal [MESH:D015674] (2735) |
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Alopecia [MESH:D000505] (1383) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Hernia, Diaphragmatic [MESH:D006548] (2647) |
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Intervertebral disc disease [MESH:C535531] (514) |
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Hepatomegaly [MESH:D006529] (1169) |
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Splenomegaly [MESH:D013163] (1258) |
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Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
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Intestinal Polyps [MESH:D007417] (1592) |
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Emphysema [MESH:D004646] (1096) |
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Growth Disorders [MESH:D006130] (2438) |
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Hyperbilirubinemia [MESH:D006932] (1860) |
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Hyperplasia [MESH:D006965] (2463) |
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Ischemia [MESH:D007511] (3049) |
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Metaplasia [MESH:D008679] (1469) |
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Neointima [MESH:D058426] (814) |
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Nerve Degeneration [MESH:D009410] (4061) |
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Torsades de Pointes [MESH:D016171] (880) |
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Translocation, Genetic [MESH:D014178] (557) |
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Disease Progression [MESH:D018450] (2868) |
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Recurrence [MESH:D012008] (830) |
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Keloid [MESH:D007627] (1110) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Cerebral Hemorrhage [MESH:D002543] (2872) |
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Subarachnoid Hemorrhage [MESH:D013345] (1081) |
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Neurogenic Inflammation [MESH:D020078] (2246) |
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Shock, Septic [MESH:D012772] (1830) |
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Endotoxemia [MESH:D019446] (1289) |
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Osteonecrosis [MESH:D010020] (537) |
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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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Pain, Postoperative [MESH:D010149] (529) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Multiple Organ Failure [MESH:D009102] (1836) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Shock, Septic [MESH:D012772] (1830) |
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Cyanosis [MESH:D003490] (288) |
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Edema [MESH:D004487] (3726) |
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Feminization [MESH:D005262] (655) |
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Fever [MESH:D005334] (2856) |
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Hypothermia [MESH:D007035] (2075) |
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Weight Gain [MESH:D015430] (2595) |
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Cachexia [MESH:D002100] (2283) |
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Obesity [MESH:D009765] (4454) |
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Seizures [MESH:D012640] (4502) |
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Catalepsy [MESH:D002375] (1429) |
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Hyperkinesis [MESH:D006948] (1799) |
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Hypokinesia [MESH:D018476] (279) |
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Memory Disorders [MESH:D008569] (3233) |
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Intellectual Disability [MESH:D008607] (1476) |
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Learning Disorders [MESH:D007859] (2727) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Neuralgia [MESH:D009437] (2074) |
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Gastroparesis [MESH:D018589] (732) |
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Marshall syndrome [MESH:C536025] (52) |
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Hyperalgesia [MESH:D006930] (3929) |
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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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Nausea [MESH:D009325] (2300) |
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Vomiting [MESH:D014839] (1354) |
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Respiratory Sounds [MESH:D012135] (713) |
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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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Dermatitis, Occupational [MESH:D009783] (311) |
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Asbestosis [MESH:D001195] (935) |
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Berylliosis [MESH:D001607] (2005) |
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Silicosis [MESH:D012829] (1273) |
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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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Stevens-Johnson Syndrome [MESH:D013262] (1163) |
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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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Psychoses, Substance-Induced [MESH:D011605] (2053) |
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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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Psychoses, Substance-Induced [MESH:D011605] (2052) |
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Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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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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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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D02. Organic Chemicals |
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D02. Organic Chemicals |
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Acetamides [MESH:D000081] (492) |
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Acetamides [MESH:D000081] (397) |
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