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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selectin E [HGNC:SELE] (94) |
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cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612) |
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interleukin 01, beta [HGNC:IL1B] (497) |
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nuclear receptor subfamily 1, group I, member 2 [HGNC:NR1I2] (328) |
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tumor necrosis factor [HGNC:TNF] (795) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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activity (2865) |
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expression (3238) |
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reaction (1574) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Chlamydia Infections [MESH:D002690] (1696) |
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Salmonella Infections, Animal [MESH:D012481] (604) |
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Legionnaires' Disease [MESH:D007877] (611) |
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Listeriosis [MESH:D008088] (1622) |
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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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Appendicitis [MESH:D001064] (774) |
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Peritonitis [MESH:D010538] (800) |
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Shock, Septic [MESH:D012772] (1830) |
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Chlamydia Infections [MESH:D002690] (1693) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Hepatitis B [MESH:D006509] (976) |
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Hepatitis B [MESH:D006509] (976) |
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Hepatitis C [MESH:D006526] (1627) |
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Hepatitis C [MESH:D006526] (1627) |
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Respiratory Syncytial Virus Infections [MESH:D018357] (852) |
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Cardiovirus Infections [MESH:D018188] (1548) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Trichuriasis [MESH:D014257] (805) |
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Malaria [MESH:D008288] (2175) |
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Entamoebiasis [MESH:D004749] (1689) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
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Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
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C04. Neoplasms |
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C04. Neoplasms |
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Neoplasms, Experimental [MESH:D009374] (5218) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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Osteosarcoma [MESH:D012516] (2175) |
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Fibromatosis, Aggressive [MESH:D018222] (1562) |
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Rhabdomyoma [MESH:D012207] (200) |
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Osteosarcoma [MESH:D012516] (2175) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Mesothelioma [MESH:D008654] (2567) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Mesothelioma [MESH:D008654] (2567) |
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Glioblastoma [MESH:D005909] (2554) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Melanoma [MESH:D008545] (3508) |
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Breast Neoplasms [MESH:D001943] (6077) |
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Soft Tissue Neoplasms [MESH:D012983] (2003) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Lung Neoplasms [MESH:D008175] (6015) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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ACTH Syndrome, Ectopic [MESH:D000182] (200) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Craniosynostoses [MESH:D003398] (438) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Osteolysis [MESH:D010014] (1787) |
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Femur Head Necrosis [MESH:D005271] (268) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Synovitis [MESH:D013585] (270) |
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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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Chondrocalcinosis [MESH:D002805] (213) |
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Sacroiliitis [MESH:D058566] (202) |
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Arthritis, Gouty [MESH:D015210] (211) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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MELAS Syndrome [MESH:D017241] (1061) |
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MERRF Syndrome [MESH:D017243] (1053) |
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Kearns-Sayre Syndrome [MESH:D007625] (1054) |
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Dermatomyositis [MESH:D003882] (1826) |
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Dermatomyositis [MESH:D003882] (1826) |
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Craniosynostoses [MESH:D003398] (438) |
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Craniosynostoses [MESH:D003398] (438) |
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Craniosynostoses [MESH:D003398] (438) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Arthritis, Gouty [MESH:D015210] (211) |
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C06. Digestive System Diseases |
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C06. Digestive System Diseases |
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Cholestasis [MESH:D002779] (3419) |
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Gallstones [MESH:D042882] (350) |
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Gallstones [MESH:D042882] (350) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Appendicitis [MESH:D001064] (774) |
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Mucositis [MESH:D052016] (1238) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Gastritis, Atrophic [MESH:D005757] (947) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Appendicitis [MESH:D001064] (774) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Peptic Ulcer [MESH:D010437] (1969) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colorectal Neoplasms [MESH:D015179] (4534) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Gastritis, Atrophic [MESH:D005757] (947) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Fatty Liver [MESH:D005234] (3584) |
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Hepatic Encephalopathy [MESH:D006501] (1795) |
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Liver Failure, Acute [MESH:D017114] (2404) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Hepatitis B [MESH:D006509] (976) |
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Hepatitis C [MESH:D006526] (1627) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Peritonitis [MESH:D010538] (800) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Facial Paralysis [MESH:D005158] (238) |
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Mucositis [MESH:D052016] (1238) |
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Oral Submucous Fibrosis [MESH:D009914] (2432) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Not Fully Specified [NFS] (1984) |
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Asthma [MESH:D001249] (4098) |
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Bronchiectasis [MESH:D001987] (1792) |
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Bronchiolitis Obliterans [MESH:D001989] (611) |
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Lung Neoplasms [MESH:D008175] (6012) |
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Pneumonia [MESH:D011014] (3482) |
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Pulmonary Edema [MESH:D011654] (2109) |
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Pulmonary Fibrosis [MESH:D011658] (3140) |
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Anthracosis [MESH:D055008] (1805) |
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Berylliosis [MESH:D001607] (2005) |
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Asthma [MESH:D001249] (3903) |
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Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564) |
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Bronchiolitis Obliterans [MESH:D001989] (611) |
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Anthracosis [MESH:D055008] (1805) |
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Berylliosis [MESH:D001607] (2005) |
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Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
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Pleurisy [MESH:D010998] (2070) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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Asthma [MESH:D001249] (4098) |
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Pleurisy [MESH:D010998] (2070) |
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Pneumonia [MESH:D011014] (3482) |
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Legionnaires' Disease [MESH:D007877] (611) |
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Lung Neoplasms [MESH:D008175] (6013) |
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C09. Otorhinolaryngologic Diseases |
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C09. Otorhinolaryngologic Diseases |
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Deafness [MESH:D003638] (623) |
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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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Restless Legs Syndrome [MESH:D012148] (379) |
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Myasthenia Gravis [MESH:D009157] (632) |
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Multiple Sclerosis [MESH:D009103] (1716) |
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Brain Injuries [MESH:D001930] (3429) |
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Parkinson Disease [MESH:D010300] (3595) |
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Cerebral Palsy [MESH:D002547] (300) |
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Hepatic Encephalopathy [MESH:D006501] (1795) |
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MELAS Syndrome [MESH:D017241] (1061) |
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MERRF Syndrome [MESH:D017243] (1053) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Brain Ischemia [MESH:D002545] (4873) |
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Stroke [MESH:D020521] (3702) |
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MELAS Syndrome [MESH:D017241] (1061) |
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Cerebral Hemorrhage [MESH:D002543] (2873) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Seizures [MESH:D012640] (4502) |
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Status Epilepticus [MESH:D013226] (4014) |
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MERRF Syndrome [MESH:D017243] (1053) |
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Epilepsy, Tonic-Clonic [MESH:D004830] (1042) |
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Spasms, Infantile [MESH:D013036] (468) |
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Migraine Disorders [MESH:D008881] (2318) |
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Pituitary ACTH Hypersecretion [MESH:D047748] (599) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Parkinson Disease [MESH:D010300] (3595) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Spinal Cord Compression [MESH:D013117] (1800) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
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Kearns-Sayre Syndrome [MESH:D007625] (1054) |
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Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
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Multiple Sclerosis [MESH:D009103] (1716) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Neural Tube Defects [MESH:D009436] (2143) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Parkinson Disease [MESH:D010300] (3595) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Neurogenic Inflammation [MESH:D020078] (2246) |
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Seizures [MESH:D012640] (4514) |
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Catalepsy [MESH:D002375] (1429) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Lethargy [MESH:D053609] (1035) |
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Learning Disorders [MESH:D007859] (2727) |
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Amnesia [MESH:D000647] (1911) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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Neuralgia [MESH:D009437] (2074) |
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Facial Paralysis [MESH:D005158] (238) |
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Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
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Deafness [MESH:D003638] (623) |
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Hyperalgesia [MESH:D006930] (3929) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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MELAS Syndrome [MESH:D017241] (1061) |
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MERRF Syndrome [MESH:D017243] (1053) |
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Kearns-Sayre Syndrome [MESH:D007625] (1054) |
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Dermatomyositis [MESH:D003882] (1826) |
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Dermatomyositis [MESH:D003882] (1826) |
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Myasthenia Gravis [MESH:D009157] (632) |
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Neuralgia [MESH:D009437] (2078) |
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Tangier Disease [MESH:D013631] (170) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Manganese Poisoning [MESH:D020149] (2214) |
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Restless Legs Syndrome [MESH:D012148] (379) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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Restless Legs Syndrome [MESH:D012148] (379) |
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Brain Injuries [MESH:D001930] (3431) |
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C11. Eye Diseases |
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C11. Eye Diseases |
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Not Fully Specified [NFS] (245) |
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Eyelid Diseases [MESH:D005141] (882) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
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Eye Pain [MESH:D058447] (207) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Myopia [MESH:D009216] (349) |
|
|
|
|
|
|
|
|
|
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
Penile Diseases [MESH:D010409] (1805) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
Diabetes Insipidus [MESH:D003919] (354) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
|
|
|
Kidney Tubular Necrosis, Acute [MESH:D007683] (974) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Cystitis [MESH:D003556] (604) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Hematuria [MESH:D006417] (477) |
|
|
Oliguria [MESH:D009846] (307) |
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
|
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
 |
C13. Female Urogenital Diseases and Pregnancy Complications |
 |
 |
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
|
|
|
|
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
Diabetes Insipidus [MESH:D003919] (354) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
|
|
|
Kidney Tubular Necrosis, Acute [MESH:D007683] (974) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Cystitis [MESH:D003556] (604) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Hematuria [MESH:D006417] (477) |
|
|
Oliguria [MESH:D009846] (307) |
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
|
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Placenta Diseases [MESH:D010922] (1781) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Ventricular Dysfunction [MESH:D018754] (2348) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Long QT Syndrome [MESH:D008133] (693) |
|
|
Sick Sinus Syndrome [MESH:D012804] (293) |
|
|
Sick Sinus Syndrome [MESH:D012804] (293) |
|
|
|
|
|
Torsades de Pointes [MESH:D016171] (880) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1516) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Myocarditis [MESH:D009205] (1708) |
|
|
|
|
|
|
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1451) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
|
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
|
|
|
Aortic Stenosis, Subvalvular [MESH:D001020] (203) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Reperfusion Injury [MESH:D015427] (4968) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
|
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Brain Ischemia [MESH:D002545] (4873) |
|
|
Stroke [MESH:D020521] (3702) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Thrombosis [MESH:D013927] (3101) |
|
|
Hypertension, Essential [MESH:C562386] (1308) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
|
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
|
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
|
|
|
|
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
|
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Leukocytosis [MESH:D007964] (988) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
Job Syndrome [MESH:D007589] (772) |
|
|
Lymphoproliferative Disorders [MESH:D008232] (4638) |
|
|
Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
|
|
|
|
|
|
Long QT Syndrome [MESH:D008133] (693) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Craniosynostoses [MESH:D003398] (438) |
|
|
Craniosynostoses [MESH:D003398] (438) |
|
|
Craniosynostoses [MESH:D003398] (438) |
|
|
Neural Tube Defects [MESH:D009436] (2143) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
|
|
|
Familial HDL deficiency [MESH:C538394] (170) |
|
|
Tangier Disease [MESH:D013631] (170) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Arthritis, Gouty [MESH:D015210] (211) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
|
|
|
Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Breast Neoplasms [MESH:D001943] (6077) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Hirsutism [MESH:D006628] (323) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
|
|
|
|
|
|
|
|
|
Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
|
|
|
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) |
|
|
Urticaria [MESH:D014581] (2668) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Hypocalcemia [MESH:D006996] (378) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hypoglycemia [MESH:D007003] (2420) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
|
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
|
|
|
Familial HDL deficiency [MESH:C538394] (170) |
|
|
Tangier Disease [MESH:D013631] (170) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
|
|
|
Familial HDL deficiency [MESH:C538394] (170) |
|
|
Tangier Disease [MESH:D013631] (170) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Arthritis, Gouty [MESH:D015210] (211) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Hypophosphatemia [MESH:D017674] (640) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Hypernatremia [MESH:D006955] (215) |
|
|
Hypocalcemia [MESH:D006996] (368) |
|
|
Hypokalemia [MESH:D007008] (1041) |
|
|
Hyponatremia [MESH:D007010] (789) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Proopiomelanocortin Deficiency [MESH:C565726] (200) |
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Obesity, Morbid [MESH:D009767] (515) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
Adrenal Cortex Diseases [MESH:D000303] (969) |
|
|
Proopiomelanocortin Deficiency [MESH:C565726] (200) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Cushing Syndrome [MESH:D003480] (282) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Pancreatic Neoplasms [MESH:D010190] (3820) |
|
|
|
|
|
|
|
|
|
|
|
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
|
|
Diabetes Insipidus [MESH:D003919] (302) |
|
|
Pituitary ACTH Hypersecretion [MESH:D047748] (599) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
Not Fully Specified [NFS] (350) |
|
|
Graft vs Host Disease [MESH:D006086] (674) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Myasthenia Gravis [MESH:D009157] (632) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Drug Hypersensitivity [MESH:D004342] (4000) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Job Syndrome [MESH:D007589] (772) |
|
|
Lymphoproliferative Disorders [MESH:D008232] (4734) |
|
 |
C22. Animal Diseases |
 |
 |
|
C22. Animal Diseases |
|
|
Disease Models, Animal [MESH:D004195] (2058) |
|
|
Salmonella Infections, Animal [MESH:D012481] (604) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
|
|
|
Gallstones [MESH:D042882] (350) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Hernia, Diaphragmatic [MESH:D006548] (2647) |
|
|
Cardiomegaly [MESH:D006332] (3802) |
|
|
Fibrosis [MESH:D005355] (3133) |
|
|
Gliosis [MESH:D005911] (1419) |
|
|
Hyperbilirubinemia [MESH:D006932] (1860) |
|
|
Leukocytosis [MESH:D007964] (978) |
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Nerve Degeneration [MESH:D009410] (4061) |
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Atrial Fibrillation [MESH:D001281] (1053) |
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Bradycardia [MESH:D001919] (1899) |
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Long QT Syndrome [MESH:D008133] (691) |
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Sick Sinus Syndrome [MESH:D012804] (293) |
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Sick Sinus Syndrome [MESH:D012804] (293) |
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Torsades de Pointes [MESH:D016171] (880) |
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Disease Progression [MESH:D018450] (2868) |
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Recurrence [MESH:D012008] (830) |
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Hematuria [MESH:D006417] (477) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Cerebral Hemorrhage [MESH:D002543] (2872) |
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Neurogenic Inflammation [MESH:D020078] (2246) |
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Shock, Septic [MESH:D012772] (1830) |
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Femur Head Necrosis [MESH:D005271] (266) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Reperfusion Injury [MESH:D015427] (4968) |
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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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Chills [MESH:D023341] (644) |
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Edema [MESH:D004487] (3726) |
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Fever [MESH:D005334] (2856) |
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Hypothermia [MESH:D007035] (2075) |
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Weight Gain [MESH:D015430] (2595) |
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Cachexia [MESH:D002100] (2283) |
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Proopiomelanocortin Deficiency [MESH:C565726] (200) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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Obesity, Morbid [MESH:D009767] (515) |
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Eye Pain [MESH:D058447] (207) |
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Seizures [MESH:D012640] (4502) |
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Sleep Disorders [MESH:D012893] (1301) |
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Catalepsy [MESH:D002375] (1429) |
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Lethargy [MESH:D053609] (1035) |
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Intellectual Disability [MESH:D008607] (1476) |
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Learning Disorders [MESH:D007859] (2727) |
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Amnesia [MESH:D000647] (1911) |
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Neuralgia [MESH:D009437] (2074) |
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Facial Paralysis [MESH:D005158] (238) |
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Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
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Deafness [MESH:D003638] (593) |
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Hyperalgesia [MESH:D006930] (3929) |
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Eye Pain [MESH:D058447] (207) |
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Neuralgia [MESH:D009437] (2074) |
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Acute Coronary Syndrome [MESH:D054058] (2286) |
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Angina, Stable [MESH:D060050] (1702) |
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Constipation [MESH:D003248] (506) |
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Nausea [MESH:D009325] (2300) |
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Vomiting [MESH:D014839] (1354) |
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Anoxia [MESH:D000860] (1698) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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Hypercalciuria [MESH:D053565] (330) |
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Oliguria [MESH:D009846] (307) |
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Albuminuria [MESH:D000419] (2394) |
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Hirsutism [MESH:D006628] (323) |
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C24. Occupational Diseases |
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C24. Occupational Diseases |
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Berylliosis [MESH:D001607] (2005) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug Hypersensitivity [MESH:D004342] (4001) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Manganese Poisoning [MESH:D020149] (2214) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Tobacco Use Disorder [MESH:D014029] (628) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Heroin Dependence [MESH:D006556] (950) |
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C26. Wounds and Injuries |
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C26. Wounds and Injuries |
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Not Fully Specified [NFS] (2454) |
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Burns [MESH:D002056] (2565) |
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Vascular System Injuries [MESH:D057772] (2086) |
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Brain Injuries [MESH:D001930] (3431) |
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Radiation Injuries, Experimental [MESH:D011833] (2662) |
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Spinal Cord Compression [MESH:D013117] (1800) |
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Brain Injuries [MESH:D001930] (3431) |
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D02. Organic Chemicals |
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D02. Organic Chemicals |
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Lovastatin [MESH:D008148] (21) |
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D04. Polycyclic Compounds |
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D04. Polycyclic Compounds |
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Lovastatin [MESH:D008148] (21) |
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D27. Chemical Actions and Uses |
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D27. Chemical Actions and Uses |
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Hydroxymethylglutaryl-CoA Reductase Inhibitors [MESH:D019161] (7) |
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Hydroxymethylglutaryl-CoA Reductase Inhibitors [MESH:D019161] (7) |
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Anti-Bacterial Agents [MESH:D000900] (107) |
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Antifungal Agents [MESH:D000935] (55) |
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Hydroxymethylglutaryl-CoA Reductase Inhibitors [MESH:D019161] (7) |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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Proopiomelanocortin Deficiency [MESH:C565726] (200) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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G. Phenomena and Processes |
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G. Phenomena and Processes |
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Proopiomelanocortin Deficiency [MESH:C565726] (200) |
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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) |
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