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 of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [HGNC:NFKBIA] (290) |
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MAX dimerization protein 1 [HGNC:MXD1] (46) |
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X-box binding protein 1 [HGNC:XBP1] (79) |
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chemokine (C-X-C motif) receptor 04 [HGNC:CXCR4] (92) |
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prion protein [HGNC:PRNP] (49) |
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chemokine (C-X-C motif) receptor 04 [HGNC:CXCR4] (92) |
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cytochrome P450, family 01, subfamily B, polypeptide 01 [HGNC:CYP1B1] (301) |
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interleukin 08 [HGNC:IL8] (649) |
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interferon gamma receptor 2 (interferon gamma transducer 1) [HGNC:IFNGR2] (24) |
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glutathione S-transferase pi 1 [HGNC:GSTP1] (218) |
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heat shock 70kDa protein 05 (glucose-regulated protein, 78kDa) [HGNC:HSPA5] (148) |
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interferon gamma receptor 2 (interferon gamma transducer 1) [HGNC:IFNGR2] (24) |
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interleukin 08 [HGNC:IL8] (649) |
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MAX dimerization protein 1 [HGNC:MXD1] (46) |
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mitogen-activated protein kinase kinase kinase 8 [HGNC:MAP3K8] (33) |
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tumor necrosis factor, alpha-induced protein 3 [HGNC:TNFAIP3] (88) |
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pellino E3 ubiquitin protein ligase 1 [HGNC:PELI1] (20) |
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prostaglandin E receptor 2 (subtype EP2), 53kDa [HGNC:PTGER2] (29) |
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solute carrier family 07 (anionic amino acid transporter light chain, xc- system), member 11 [HGNC:SLC7A11] (77) |
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interferon-induced protein with tetratricopeptide repeats 1 [HGNC:IFIT1] (45) |
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interferon-induced protein with tetratricopeptide repeats 2 [HGNC:IFIT2] (31) |
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interferon-induced protein with tetratricopeptide repeats 3 [HGNC:IFIT3] (35) |
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neutrophil cytosolic factor 2 [HGNC:NCF2] (39) |
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early growth response 3 [HGNC:EGR3] (37) |
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human immunodeficiency virus type I enhancer binding protein 2 [HGNC:HIVEP2] (23) |
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zinc finger, CCHC domain containing 2 [HGNC:ZCCHC2] (25) |
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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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activity (2549) |
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expression (2187) |
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reaction (3393) |
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activity (2865) |
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expression (3238) |
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A. Anatomy |
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A. Anatomy |
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Peters anomaly [MESH:C537884] (465) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Mycoplasma Infections [MESH:D009175] (1947) |
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Mycobacterium Infections, Nontuberculous [MESH:D009165] (480) |
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Sepsis [MESH:D018805] (3556) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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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 C [MESH:D006526] (1627) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Hepatitis C [MESH:D006526] (1627) |
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Influenza, Human [MESH:D007251] (1075) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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HIV Infections [MESH:D015658] (3296) |
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WHIM syndrome [MESH:C536697] (148) |
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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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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
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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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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510) |
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Lymphoma, Follicular [MESH:D008224] (1025) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
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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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Leiomyosarcoma [MESH:D007890] (977) |
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Leiomyosarcoma [MESH:D007890] (977) |
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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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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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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 Esophagus [MESH:C562730] (1530) |
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Adenocarcinoma, Clear Cell [MESH:D018262] (1291) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Cholangiocarcinoma [MESH:D018281] (2398) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Glioblastoma [MESH:D005909] (2554) |
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Papilloma [MESH:D010212] (2243) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Multiple Myeloma [MESH:D009101] (2767) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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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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Pancreatic Neoplasms [MESH:D010190] (3820) |
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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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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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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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Pituitary Neoplasms [MESH:D010911] (914) |
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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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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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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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Leukoplakia, Oral [MESH:D007972] (921) |
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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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Bone Neoplasms [MESH:D001859] (1334) |
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Osteochondrodysplasias [MESH:D010009] (2440) |
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Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140) |
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Kowarski syndrome [MESH:C537505] (129) |
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Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129) |
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Short Stature, Idiopathic, Autosomal [MESH:C565805] (194) |
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Acromegaly [MESH:D000172] (466) |
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Kowarski syndrome [MESH:C537505] (129) |
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Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129) |
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Short Stature, Idiopathic, Autosomal [MESH:C565805] (194) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
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Craniofacial Abnormalities [MESH:D019465] (3098) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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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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Pancreatic Neoplasms [MESH:D010190] (3820) |
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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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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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Esophagitis, Peptic [MESH:D004942] (709) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Esophagitis, Peptic [MESH:D004942] (709) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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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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Colitis, Ulcerative [MESH:D003093] (2601) |
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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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Duodenal Ulcer [MESH:D004381] (1549) |
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Esophagitis, Peptic [MESH:D004942] (709) |
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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) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Fatty Liver [MESH:D005234] (3584) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Hepatorenal Syndrome [MESH:D006530] (910) |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Hepatitis C [MESH:D006526] (1627) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Pancreatitis [MESH:D010195] (1924) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Behcet Syndrome [MESH:D001528] (1784) |
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Oral Submucous Fibrosis [MESH:D009914] (2432) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80) |
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Hypertension, Pulmonary [MESH:D006976] (2000) |
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Lung Injury [MESH:D055370] (3688) |
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Pneumonia [MESH:D011014] (3482) |
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Pulmonary Fibrosis [MESH:D011658] (3140) |
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Asthma [MESH:D001249] (3903) |
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Pulmonary Emphysema [MESH:D011656] (1259) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80) |
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Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80) |
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Influenza, Human [MESH:D007251] (1075) |
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Pneumonia [MESH:D011014] (3482) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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C09. Otorhinolaryngologic Diseases |
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C09. Otorhinolaryngologic Diseases |
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Hearing Loss, Noise-Induced [MESH:D006317] (134) |
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Vestibular Diseases [MESH:D015837] (819) |
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Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80) |
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C10. Nervous System Diseases |
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C10. Nervous System Diseases |
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Not Fully Specified [NFS] (4027) |
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Multiple Sclerosis [MESH:D009103] (1716) |
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Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
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Brain Injuries [MESH:D001930] (3429) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Huntington Disease-Like 1 [MESH:C566398] (98) |
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Parkinson Disease [MESH:D010300] (3595) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Pituitary Neoplasms [MESH:D010911] (914) |
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Carotid Artery Diseases [MESH:D002340] (1993) |
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Stroke [MESH:D020521] (3702) |
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Ischemic Attack, Transient [MESH:D002546] (1313) |
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Cerebral Hemorrhage [MESH:D002543] (2873) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Creutzfeldt-Jakob Syndrome [MESH:D007562] (118) |
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Huntington Disease-Like 1 [MESH:C566398] (98) |
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Landau-Kleffner Syndrome [MESH:D018887] (87) |
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Seizures [MESH:D012640] (4502) |
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Status Epilepticus [MESH:D013226] (4014) |
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Epilepsy, Rolandic [MESH:D019305] (107) |
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|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140) |
|
|
Acromegaly [MESH:D000172] (466) |
|
|
|
|
|
Kowarski syndrome [MESH:C537505] (129) |
|
|
Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129) |
|
|
Short Stature, Idiopathic, Autosomal [MESH:C565805] (194) |
|
|
Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
|
|
|
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98) |
|
|
Creutzfeldt-Jakob Syndrome [MESH:D007562] (118) |
|
|
Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98) |
|
|
Insomnia, Fatal Familial [MESH:D034062] (98) |
|
|
Scrapie [MESH:D012608] (462) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
|
|
|
Huntington Disease-Like 1 [MESH:C566398] (98) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
Spinal Cord Injuries [MESH:D013119] (1674) |
|
|
|
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98) |
|
|
Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Huntington Disease-Like 1 [MESH:C566398] (98) |
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98) |
|
|
Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98) |
|
|
Insomnia, Fatal Familial [MESH:D034062] (98) |
|
|
Scrapie [MESH:D012608] (462) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Ataxia [MESH:D001259] (1138) |
|
|
Memory Disorders [MESH:D008569] (3233) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Language Development Disorders [MESH:D007805] (351) |
|
|
Speech Disorders [MESH:D013064] (482) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
Pain, Intractable [MESH:D010148] (707) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
|
|
|
|
|
|
|
|
|
Hearing Loss, Noise-Induced [MESH:D006317] (134) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
|
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
|
|
|
|
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Diabetic Neuropathies [MESH:D003929] (2442) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
|
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
|
|
|
|
|
|
|
|
|
Insomnia, Fatal Familial [MESH:D034062] (98) |
|
|
Spinal Cord Injuries [MESH:D013119] (1676) |
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
|
|
|
|
|
|
Peters anomaly [MESH:C537884] (465) |
|
|
Peters anomaly [MESH:C537884] (465) |
|
|
|
|
|
Glaucoma 3, Primary Congenital, A [MESH:C565547] (434) |
|
|
Glaucoma, Primary Open Angle [MESH:C562750] (466) |
|
|
Glaucoma 1, Open Angle, A [MESH:C564234] (446) |
|
|
Retinal Degeneration [MESH:D012162] (2386) |
|
|
Retinal Detachment [MESH:D012163] (1639) |
|
|
|
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Azoospermia [MESH:D053713] (1052) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Erectile Dysfunction [MESH:D007172] (1791) |
|
|
|
|
|
|
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Azotemia [MESH:D053099] (326) |
|
|
|
|
|
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 |
|
|
|
|
|
Endometriosis [MESH:D004715] (2461) |
|
|
Infertility [MESH:D007246] (2211) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
|
|
|
|
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Azotemia [MESH:D053099] (326) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Pre-Eclampsia [MESH:D011225] (1435) |
|
|
Prenatal Exposure Delayed Effects [MESH:D011297] (870) |
|
|
Mastitis [MESH:D008413] (76) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
|
|
|
|
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
Arrhythmias, Cardiac [MESH:D001145] (4679) |
|
|
Cardiomegaly [MESH:D006332] (4081) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Heart Valve Diseases [MESH:D006349] (3333) |
|
|
Pericardial Effusion [MESH:D010490] (1015) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Infarction [MESH:D009203] (4122) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Diabetic Angiopathies [MESH:D003925] (1984) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypertension [MESH:D006973] (5655) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Peripheral Vascular Diseases [MESH:D016491] (1412) |
|
|
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) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
Stroke [MESH:D020521] (3702) |
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Thrombosis [MESH:D013927] (3101) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Infarction [MESH:D009203] (4151) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
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 |
|
|
Polycythemia [MESH:D011086] (412) |
|
|
Anemia, Hemolytic [MESH:D000743] (3083) |
|
|
|
|
|
Bernard-Soulier Syndrome [MESH:D001606] (39) |
|
|
Bernard-Soulier Syndrome [MESH:D001606] (39) |
|
|
Thrombocytopenia [MESH:D013921] (2966) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
|
|
Bernard-Soulier Syndrome [MESH:D001606] (39) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
|
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II [MESH:C565531] (85) |
|
|
|
|
|
|
|
|
|
|
|
Hemophagocytic lymphohistiocytosis, familial, 4 [MESH:C537252] (29) |
|
|
|
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
Lymphoma, Follicular [MESH:D008224] (1025) |
|
|
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) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
|
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
|
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
Peters anomaly [MESH:C537884] (465) |
|
|
Craniofacial Abnormalities [MESH:D019465] (3064) |
|
|
|
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
|
|
|
|
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
|
|
|
Bernard-Soulier Syndrome [MESH:D001606] (39) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
|
|
|
Turner Syndrome [MESH:D014424] (131) |
|
|
Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II [MESH:C565531] (85) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98) |
|
|
Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Huntington Disease-Like 1 [MESH:C566398] (98) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Gamma-cystathionase deficiency [MESH:C535408] (106) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Asphyxia Neonatorum [MESH:D001238] (1648) |
|
|
Bare lymphocyte syndrome 2 [MESH:C537079] (61) |
|
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79) |
|
|
X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
Chloracne [MESH:D054506] (1274) |
|
|
Mastitis [MESH:D008413] (76) |
|
|
Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Drug Eruptions [MESH:D003875] (2697) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
|
|
|
|
|
|
Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
|
|
|
|
|
WHIM syndrome [MESH:C536697] (148) |
|
|
Lichenoid Eruptions [MESH:D017512] (1324) |
|
|
Psoriasis [MESH:D011565] (3278) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Iron Metabolism Disorders [MESH:D019189] (2139) |
|
|
|
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Calcinosis [MESH:D002114] (2989) |
|
|
|
|
|
Bare lymphocyte syndrome 2 [MESH:C537079] (61) |
|
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79) |
|
|
Hyperglycemia [MESH:D006943] (1858) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Insulin Resistance [MESH:D007333] (3511) |
|
|
|
|
|
Gamma-cystathionase deficiency [MESH:C535408] (106) |
|
|
|
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Gamma-cystathionase deficiency [MESH:C535408] (106) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Gamma-cystathionase deficiency [MESH:C535408] (106) |
|
|
Obesity [MESH:D009765] (4462) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
Addison Disease [MESH:D000224] (40) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
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Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
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Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
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Diabetic Angiopathies [MESH:D003925] (1984) |
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Diabetic Neuropathies [MESH:D003929] (2443) |
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Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140) |
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Kowarski syndrome [MESH:C537505] (129) |
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Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129) |
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Short Stature, Idiopathic, Autosomal [MESH:C565805] (194) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Puberty, Precocious [MESH:D011629] (1147) |
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Turner Syndrome [MESH:D014424] (131) |
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Turner Syndrome [MESH:D014424] (131) |
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Ovarian Neoplasms [MESH:D010051] (3281) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140) |
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Acromegaly [MESH:D000172] (466) |
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Kowarski syndrome [MESH:C537505] (129) |
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Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129) |
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Short Stature, Idiopathic, Autosomal [MESH:C565805] (194) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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C20. Immune System Diseases |
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C20. Immune System Diseases |
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Addison Disease [MESH:D000224] (40) |
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Arthritis, Rheumatoid [MESH:D001172] (3601) |
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Glomerulonephritis, IGA [MESH:D005922] (897) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
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Pemphigoid, Bullous [MESH:D010391] (707) |
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Multiple Sclerosis [MESH:D009103] (1716) |
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Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
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Drug Eruptions [MESH:D003875] (2695) |
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Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80) |
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Dermatitis, Allergic Contact [MESH:D017449] (3241) |
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Dermatitis, Atopic [MESH:D003876] (2052) |
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Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80) |
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Asthma [MESH:D001249] (3914) |
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WHIM syndrome [MESH:C536697] (148) |
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CD8 Deficiency, Familial [MESH:C563824] (41) |
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Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II [MESH:C565531] (85) |
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Bare lymphocyte syndrome 2 [MESH:C537079] (61) |
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Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79) |
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X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42) |
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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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Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Lymphoma, Follicular [MESH:D008224] (1025) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
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Multiple Myeloma [MESH:D009101] (2765) |
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C22. Animal Diseases |
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C22. Animal Diseases |
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Scrapie [MESH:D012608] (462) |
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Muscular Atrophy [MESH:D009133] (1234) |
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Cardiomegaly [MESH:D006332] (3802) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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Intestinal Polyps [MESH:D007417] (1592) |
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Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80) |
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Arrhythmias, Cardiac [MESH:D001145] (4658) |
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Azotemia [MESH:D053099] (326) |
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Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506) |
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Fibrosis [MESH:D005355] (3133) |
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Growth Disorders [MESH:D006130] (2438) |
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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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Necrosis [MESH:D009336] (4019) |
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Nerve Degeneration [MESH:D009410] (4061) |
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Micronuclei, Chromosome-Defective [MESH:D048629] (1013) |
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Disease Progression [MESH:D018450] (2868) |
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Cerebral Hemorrhage [MESH:D002543] (2872) |
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Neurogenic Inflammation [MESH:D020078] (2246) |
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Sepsis [MESH:D018805] (3562) |
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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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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Edema [MESH:D004487] (3726) |
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Fever [MESH:D005334] (2856) |
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Weight Gain [MESH:D015430] (2595) |
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Cachexia [MESH:D002100] (2283) |
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Obesity [MESH:D009765] (4454) |
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Seizures [MESH:D012640] (4502) |
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Ataxia [MESH:D001259] (984) |
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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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Language Development Disorders [MESH:D007805] (351) |
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Speech Disorders [MESH:D013064] (482) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Pain, Intractable [MESH:D010148] (707) |
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Neuralgia, Postherpetic [MESH:D051474] (742) |
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Gastroparesis [MESH:D018589] (732) |
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Hearing Loss, Noise-Induced [MESH:D006317] (134) |
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Hyperalgesia [MESH:D006930] (3929) |
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Pain, Intractable [MESH:D010148] (707) |
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Acute Coronary Syndrome [MESH:D054058] (2286) |
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Angina, Unstable [MESH:D000789] (782) |
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Neuralgia, Postherpetic [MESH:D051474] (742) |
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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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Occupational Diseases [MESH:D009784] (3402) |
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Not Fully Specified [NFS] (1530) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Drug Eruptions [MESH:D003875] (2697) |
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Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Neurotoxicity Syndromes [MESH:D020258] (3323) |
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Psychoses, Substance-Induced [MESH:D011605] (2053) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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Psychoses, Substance-Induced [MESH:D011605] (2052) |
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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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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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Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506) |
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Spinal Cord Injuries [MESH:D013119] (2688) |
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Vascular System Injuries [MESH:D057772] (2086) |
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Brain Injuries [MESH:D001930] (3431) |
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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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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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Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98) |
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Huntington Disease-Like 1 [MESH:C566398] (98) |
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Huntington Disease-Like 1 [MESH:C566398] (98) |
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Major Affective Disorder 1 [MESH:C565111] (237) |
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Major Affective Disorder 7 [MESH:C567529] (136) |
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