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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patatin-like phospholipase domain containing 6 [HGNC:PNPLA6] (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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cotreatment (1499) |
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activity (2549) |
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reaction (3393) |
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phosphorylation (1060) |
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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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Urinary Tract Infections [MESH:D014552] (984) |
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C04. Neoplasms |
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C04. Neoplasms |
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Precancerous Conditions [MESH:D011230] (2858) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Rhabdomyoma [MESH:D012207] (200) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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Mesothelioma [MESH:D008654] (2567) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Mesothelioma [MESH:D008654] (2567) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Glioblastoma [MESH:D005909] (2554) |
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Neuroblastoma [MESH:D009447] (1420) |
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Breast Neoplasms [MESH:D001943] (6077) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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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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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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Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
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Fibrous Dysplasia of Bone [MESH:D005357] (737) |
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
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Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Femur Head Necrosis [MESH:D005271] (268) |
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Bamforth syndrome [MESH:C537901] (186) |
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Synovitis [MESH:D013585] (270) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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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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Muscle Weakness [MESH:D018908] (478) |
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Bamforth syndrome [MESH:C537901] (186) |
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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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Pancreatic Diseases [MESH:D010182] (4453) |
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Cholestasis [MESH:D002779] (3419) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Fatty Liver [MESH:D005234] (3584) |
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Hepatitis [MESH:D006505] (3883) |
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Liver Failure, Acute [MESH:D017114] (2404) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Porphyria, Acute Hepatic [MESH:C562618] (99) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Bamforth syndrome [MESH:C537901] (186) |
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Behcet Syndrome [MESH:D001528] (1784) |
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Facial Paralysis [MESH:D005158] (238) |
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Bamforth syndrome [MESH:C537901] (186) |
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Bamforth syndrome [MESH:C537901] (186) |
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Bamforth syndrome [MESH:C537901] (186) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Asthma [MESH:D001249] (4098) |
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Hypertension, Pulmonary [MESH:D006976] (2000) |
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Pneumonia [MESH:D011014] (3482) |
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Pulmonary Edema [MESH:D011654] (2109) |
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Pulmonary Embolism [MESH:D011655] (1118) |
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Asthma [MESH:D001249] (3903) |
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Acute Lung Injury [MESH:D055371] (1907) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Sleep Apnea Syndromes [MESH:D012891] (570) |
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Asthma [MESH:D001249] (4098) |
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Pneumonia [MESH:D011014] (3482) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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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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Autonomic Nervous System Diseases [MESH:D001342] (882) |
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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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Huntington Disease [MESH:D006816] (540) |
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Cerebral Palsy [MESH:D002547] (300) |
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Cerebral Hemorrhage [MESH:D002543] (2873) |
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Pituitary Apoplexy [MESH:D010899] (125) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Huntington Disease [MESH:D006816] (540) |
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Epilepsies, Myoclonic [MESH:D004831] (1344) |
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Seizures [MESH:D012640] (4502) |
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Status Epilepticus [MESH:D013226] (4014) |
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Epilepsy, Tonic-Clonic [MESH:D004830] (1042) |
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Spasms, Infantile [MESH:D013036] (468) |
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Pituitary Apoplexy [MESH:D010899] (125) |
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Pituitary ACTH Hypersecretion [MESH:D047748] (599) |
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Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
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Huntington Disease [MESH:D006816] (540) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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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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Multiple Sclerosis [MESH:D009103] (1716) |
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Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
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Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
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Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53) |
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Huntington Disease [MESH:D006816] (540) |
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Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
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Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
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Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53) |
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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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Pain [MESH:D010146] (3875) |
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Paresis [MESH:D010291] (419) |
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Seizures [MESH:D012640] (4514) |
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Ataxia [MESH:D001259] (1138) |
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Catalepsy [MESH:D002375] (1429) |
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Hyperkinesis [MESH:D006948] (1799) |
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Tremor [MESH:D014202] (840) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Psychomotor Disorders [MESH:D011596] (576) |
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Learning Disorders [MESH:D007859] (2727) |
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Amnesia [MESH:D000647] (1911) |
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Fasciculation [MESH:D005207] (204) |
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Muscle Weakness [MESH:D018908] (478) |
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Trismus [MESH:D014313] (221) |
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Facial Paralysis [MESH:D005158] (238) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Myasthenia Gravis [MESH:D009157] (632) |
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Diabetic Neuropathies [MESH:D003929] (2442) |
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Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
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Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
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Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53) |
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Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
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Lead Poisoning, Nervous System [MESH:D020263] (102) |
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Restless Legs Syndrome [MESH:D012148] (379) |
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Sleep Apnea Syndromes [MESH:D012891] (570) |
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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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Eye Pain [MESH:D058447] (207) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Retinitis [MESH:D012173] (137) |
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Behcet Syndrome [MESH:D001528] (1784) |
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C12. Male Urogenital Diseases |
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C12. Male Urogenital Diseases |
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Penile Diseases [MESH:D010409] (1805) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Infertility, Male [MESH:D007248] (2851) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Urinary Tract Infections [MESH:D014552] (984) |
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Diabetes Insipidus [MESH:D003919] (354) |
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Nephrocalcinosis [MESH:D009397] (311) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Glomerulonephritis [MESH:D005921] (3758) |
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Kidney Calculi [MESH:D007669] (455) |
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Kidney Tubular Necrosis, Acute [MESH:D007683] (974) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
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Cystitis [MESH:D003556] (604) |
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Hematuria [MESH:D006417] (477) |
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Oliguria [MESH:D009846] (307) |
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Proteinuria [MESH:D011507] (3293) |
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Kidney Calculi [MESH:D007669] (455) |
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Kidney Calculi [MESH:D007669] (455) |
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C13. Female Urogenital Diseases and Pregnancy Complications |
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C13. Female Urogenital Diseases and Pregnancy Complications |
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Endometriosis [MESH:D004715] (2461) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Urinary Tract Infections [MESH:D014552] (984) |
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Diabetes Insipidus [MESH:D003919] (354) |
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Nephrocalcinosis [MESH:D009397] (311) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Glomerulonephritis [MESH:D005921] (3758) |
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Kidney Calculi [MESH:D007669] (455) |
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Kidney Tubular Necrosis, Acute [MESH:D007683] (974) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
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Cystitis [MESH:D003556] (604) |
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Hematuria [MESH:D006417] (477) |
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Oliguria [MESH:D009846] (307) |
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Proteinuria [MESH:D011507] (3293) |
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Kidney Calculi [MESH:D007669] (455) |
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Kidney Calculi [MESH:D007669] (455) |
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Prenatal Injuries [MESH:D049188] (1314) |
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C14. Cardiovascular Diseases |
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C14. Cardiovascular Diseases |
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Cardiomegaly [MESH:D006332] (4081) |
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Heart Failure [MESH:D006333] (4058) |
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Bradycardia [MESH:D001919] (1899) |
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Long QT Syndrome [MESH:D008133] (693) |
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Tachycardia [MESH:D013610] (3339) |
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Sick Sinus Syndrome [MESH:D012804] (293) |
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Sick Sinus Syndrome [MESH:D012804] (293) |
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Cardiomyopathy, Hypertrophic [MESH:D002312] (1516) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Cardiomyopathy, Hypertrophic [MESH:D002312] (1451) |
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Myocardial Infarction [MESH:D009203] (4122) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Aortic Stenosis, Subvalvular [MESH:D001020] (203) |
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Hyperemia [MESH:D006940] (2372) |
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Hypertension [MESH:D006973] (5655) |
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Hypotension [MESH:D007022] (4045) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Cerebral Hemorrhage [MESH:D002543] (2873) |
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Pituitary Apoplexy [MESH:D010899] (125) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Pulmonary Embolism [MESH:D011655] (1118) |
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Myocardial Infarction [MESH:D009203] (4151) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Behcet Syndrome [MESH:D001528] (1784) |
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C15. Hemic and Lymphatic Diseases |
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C15. Hemic and Lymphatic Diseases |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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Abnormalities, Drug-Induced [MESH:D000014] (1024) |
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Bamforth syndrome [MESH:C537901] (186) |
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Long QT Syndrome [MESH:D008133] (693) |
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Bamforth syndrome [MESH:C537901] (186) |
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Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
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Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
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Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53) |
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Bamforth syndrome [MESH:C537901] (186) |
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Bamforth syndrome [MESH:C537901] (186) |
|
|
ACTH Deficiency, Isolated [MESH:C562707] (124) |
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|
Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
|
|
Huntington Disease [MESH:D006816] (540) |
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Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89) |
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Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89) |
|
|
Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53) |
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Butyrylcholinesterase deficiency [MESH:C537417] (176) |
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Acatalasia [MESH:D020642] (788) |
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|
|
Porphyria, Acute Hepatic [MESH:C562618] (99) |
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|
|
Arthritis, Gouty [MESH:D015210] (211) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
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|
|
|
|
Porphyria, Acute Hepatic [MESH:C562618] (99) |
|
|
Asphyxia Neonatorum [MESH:D001238] (1648) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
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C17. Skin and Connective Tissue Diseases |
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|
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|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Keratosis [MESH:D007642] (1941) |
|
|
Breast Neoplasms [MESH:D001943] (6077) |
|
|
Bamforth syndrome [MESH:C537901] (186) |
|
|
Hirsutism [MESH:D006628] (323) |
|
|
Alopecia [MESH:D000505] (1453) |
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|
|
|
|
Porphyria, Acute Hepatic [MESH:C562618] (99) |
|
|
|
|
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|
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|
Porphyria, Acute Hepatic [MESH:C562618] (99) |
|
|
Psoriasis [MESH:D011565] (3278) |
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|
Behcet Syndrome [MESH:D001528] (1784) |
|
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C18. Nutritional and Metabolic Diseases |
 |
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C18. Nutritional and Metabolic Diseases |
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|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Hypocalcemia [MESH:D006996] (378) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
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|
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
ACTH Deficiency, Isolated [MESH:C562707] (124) |
|
|
Butyrylcholinesterase deficiency [MESH:C537417] (176) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Acatalasia [MESH:D020642] (788) |
|
|
|
|
|
Porphyria, Acute Hepatic [MESH:C562618] (99) |
|
|
|
|
|
Arthritis, Gouty [MESH:D015210] (211) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
|
|
|
Porphyria, Acute Hepatic [MESH:C562618] (99) |
|
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Porphyria, Acute Hepatic [MESH:C562618] (99) |
|
|
Hypernatremia [MESH:D006955] (215) |
|
|
Hypocalcemia [MESH:D006996] (368) |
|
|
Hypokalemia [MESH:D007008] (1041) |
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Protein Deficiency [MESH:D011488] (1057) |
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Proopiomelanocortin Deficiency [MESH:C565726] (200) |
|
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C19. Endocrine System Diseases |
 |
 |
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C19. Endocrine System Diseases |
|
|
ACTH Deficiency, Isolated [MESH:C562707] (124) |
|
|
Adrenal Cortex Diseases [MESH:D000303] (969) |
|
|
Proopiomelanocortin Deficiency [MESH:C565726] (200) |
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|
Cushing Syndrome [MESH:D003480] (282) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
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Diabetic Neuropathies [MESH:D003929] (2443) |
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Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
|
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Puberty, Delayed [MESH:D011628] (449) |
|
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Diabetes Insipidus [MESH:D003919] (302) |
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Pituitary Apoplexy [MESH:D010899] (125) |
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Pituitary ACTH Hypersecretion [MESH:D047748] (599) |
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Bamforth syndrome [MESH:C537901] (186) |
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Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) |
|
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C20. Immune System Diseases |
 |
 |
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C20. Immune System Diseases |
|
|
Not Fully Specified [NFS] (350) |
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Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
|
|
Myasthenia Gravis [MESH:D009157] (632) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
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Asthma [MESH:D001249] (3914) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Alopecia [MESH:D000505] (1383) |
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Kidney Calculi [MESH:D007669] (455) |
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Cardiomegaly [MESH:D006332] (3802) |
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Muscle Weakness [MESH:D018908] (478) |
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Bradycardia [MESH:D001919] (1899) |
|
|
Long QT Syndrome [MESH:D008133] (691) |
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Tachycardia [MESH:D013610] (3339) |
|
|
Sick Sinus Syndrome [MESH:D012804] (293) |
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Sick Sinus Syndrome [MESH:D012804] (293) |
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Sudden Infant Death [MESH:D013398] (268) |
|
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Disease Progression [MESH:D018450] (2868) |
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Recurrence [MESH:D012008] (830) |
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|
Genetic Predisposition to Disease [MESH:D020022] (966) |
|
|
Hematuria [MESH:D006417] (477) |
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|
Cerebral Hemorrhage [MESH:D002543] (2872) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
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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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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
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) |
|
|
Weight Loss [MESH:D015431] (2512) |
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Proopiomelanocortin Deficiency [MESH:C565726] (200) |
|
|
Eye Pain [MESH:D058447] (207) |
|
|
Pain [MESH:D010146] (3869) |
|
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Paresis [MESH:D010291] (419) |
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|
Seizures [MESH:D012640] (4502) |
|
|
Sleep Disorders [MESH:D012893] (1301) |
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Ataxia [MESH:D001259] (984) |
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Catalepsy [MESH:D002375] (1429) |
|
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Hyperkinesis [MESH:D006948] (1799) |
|
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Tremor [MESH:D014202] (840) |
|
|
Psychomotor Disorders [MESH:D011596] (576) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Fasciculation [MESH:D005207] (204) |
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|
Muscle Weakness [MESH:D018908] (478) |
|
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Trismus [MESH:D014313] (221) |
|
|
Facial Paralysis [MESH:D005158] (238) |
|
|
Chest Pain [MESH:D002637] (2642) |
|
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Eye Pain [MESH:D058447] (207) |
|
|
Anorexia [MESH:D000855] (854) |
|
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Constipation [MESH:D003248] (506) |
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Nausea [MESH:D009325] (2300) |
|
|
Anoxia [MESH:D000860] (1698) |
|
|
Apnea [MESH:D001049] (415) |
|
|
Hypercalciuria [MESH:D053565] (330) |
|
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Oliguria [MESH:D009846] (307) |
|
|
Proteinuria [MESH:D011507] (3293) |
|
|
Hirsutism [MESH:D006628] (323) |
|
 |
C25. Chemically-Induced Disorders |
 |
 |
|
C25. Chemically-Induced Disorders |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Foodborne Diseases [MESH:D005517] (269) |
|
|
Organophosphate Poisoning [MESH:D062025] (497) |
|
|
Psychoses, Substance-Induced [MESH:D011605] (2053) |
|
|
Lead Poisoning, Nervous System [MESH:D020263] (102) |
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Amphetamine-Related Disorders [MESH:D019969] (2858) |
|
|
Cocaine-Related Disorders [MESH:D019970] (3054) |
|
|
Psychoses, Substance-Induced [MESH:D011605] (2052) |
|
|
Substance Withdrawal Syndrome [MESH:D013375] (2956) |
|
|
Alcoholism [MESH:D000437] (1519) |
|
|
|
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Heroin Dependence [MESH:D006556] (950) |
|
 |
C26. Wounds and Injuries |
 |
 |
|
C26. Wounds and Injuries |
|
|
Burns [MESH:D002056] (2565) |
|
|
Brain Injuries [MESH:D001930] (3431) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
D02. Organic Chemicals |
 |
 |
|
D02. Organic Chemicals |
|
|
|
|
|
Organothiophosphorus Compounds [MESH:D009946] (291) |
|
|
Organothiophosphorus Compounds [MESH:D009946] (291) |
|
 |
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
 |
 |
|
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
|
|
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|
|
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|
Proopiomelanocortin Deficiency [MESH:C565726] (200) |
|
 |
G. Phenomena and Processes |
 |
 |
|
G. Phenomena and Processes |
|
|
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|
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|
|
Proopiomelanocortin Deficiency [MESH:C565726] (200) |
|
 |