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 methamidophos
C014655
 
  
  
  

MeSH Unique Identifier: C014655
Chemical – Gene Interaction

Note 1: Asoxime chloride inhibits the reaction [methamidophos results in decreased activity of ACHE protein]

Note 2: HLo 7 inhibits the reaction [methamidophos results in decreased activity of ACHE protein]

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C04. Neoplasms: Neoplasms [MESH:D009369] > Neoplasms by Histologic Type [MESH:D009370]
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C23. Pathological Conditions, Signs and Symptoms: Signs and Symptoms [MESH:D012816] > Neurologic Manifestations [MESH:D009461] > Dyskinesias [MESH:D020820] > Tremor [MESH:D014202]
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more general categories    information about this item
1. Human Genes 
1. Human Genes
 Patatin-like phospholipase domain containing [HGNC:PNPLA] (44) 
 patatin-like phospholipase domain containing 6 [HGNC:PNPLA6] (25)
2. Interaction: Human Genes and Chemicals 
2. Interaction: Human Genes and Chemicals
 Affects (3990) 
 binding (2423)
 cotreatment (1499)
 Decreases (5154) 
 activity (2549)
 reaction (3393)
 Increases (5571) 
 phosphorylation (1060)
 reaction (1574)
C01. Bacterial Infections and Mycoses 
C01. Bacterial Infections and Mycoses
 Infection [MESH:D007239] (4109) 
 Urinary Tract Infections [MESH:D014552] (984)
C04. Neoplasms 
C04. Neoplasms
 Neoplasms [MESH:D009369] (10293) 
 Precancerous Conditions [MESH:D011230] (2858)
 Neoplasms by Histologic Type [MESH:D009370] (8793) 
 Lymphoma [MESH:D008223] (3686) 
 Lymphoma, Non-Hodgkin [MESH:D008228] (3337) 
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742) 
 Neoplasms, Muscle Tissue [MESH:D009379] (1965) 
 Myoma [MESH:D009214] (203) 
 Rhabdomyoma [MESH:D012207] (200)
 Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126) 
 Neuroectodermal Tumors [MESH:D017599] (5066) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neoplasms, Glandular and Epithelial [MESH:D009375] (7760) 
 Adenoma [MESH:D000236] (4051) 
 Mesothelioma [MESH:D008654] (2567)
 Carcinoma [MESH:D002277] (7263) 
 Adenocarcinoma [MESH:D000230] (6565) 
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Carcinoma, Squamous Cell [MESH:D002294] (4294) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Neoplasms, Mesothelial [MESH:D018301] (2569) 
 Mesothelioma [MESH:D008654] (2567)
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neoplasms, Squamous Cell [MESH:D018307] (4457) 
 Carcinoma, Squamous Cell [MESH:D002294] (4294) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Neoplasms, Nerve Tissue [MESH:D009380] (5201) 
 Neuroectodermal Tumors [MESH:D017599] (5059) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Astrocytoma [MESH:D001254] (2692) 
 Glioblastoma [MESH:D005909] (2554)
 Neuroectodermal Tumors, Primitive [MESH:D018242] (2005) 
 Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433) 
 Neuroblastoma [MESH:D009447] (1420)
 Neoplasms by Site [MESH:D009371] (9169) 
 Breast Neoplasms [MESH:D001943] (6077)
 Digestive System Neoplasms [MESH:D004067] (7487) 
 Gastrointestinal Neoplasms [MESH:D005770] (6452) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Liver Neoplasms [MESH:D008113] (6048) 
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Head and Neck Neoplasms [MESH:D006258] (4612) 
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Nervous System Neoplasms [MESH:D009423] (3130) 
 Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218) 
 Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)
 Thoracic Neoplasms [MESH:D013899] (6032) 
 Respiratory Tract Neoplasms [MESH:D012142] (6020) 
 Lung Neoplasms [MESH:D008175] (6015) 
 Bronchial Neoplasms [MESH:D001984] (3608) 
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Urogenital Neoplasms [MESH:D014565] (7002) 
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Prostatic Neoplasms [MESH:D011471] (6135)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Neoplastic Processes [MESH:D009385] (5317) 
 Neoplasm Invasiveness [MESH:D009361] (3388)
 Neoplasm Metastasis [MESH:D009362] (4441)
 Carcinogenesis [MESH:D063646] (3391) 
 Cell Transformation, Neoplastic [MESH:D002471] (3389)
 Paraneoplastic Syndromes [MESH:D010257] (231) 
 Paraneoplastic Endocrine Syndromes [MESH:D009384] (207) 
 ACTH Syndrome, Ectopic [MESH:D000182] (200)
 Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218) 
 Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)
C05. Musculoskeletal Diseases 
C05. Musculoskeletal Diseases
 Musculoskeletal Diseases [MESH:D009140] (8705) 
 Bone Diseases [MESH:D001847] (5801) 
 Bone Diseases, Developmental [MESH:D001848] (3315) 
 Dwarfism [MESH:D004392] (778) 
 Congenital Hypothyroidism [MESH:D003409] (266) 
 Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)
 Osteochondrodysplasias [MESH:D010009] (2440) 
 Fibrous Dysplasia of Bone [MESH:D005357] (737)
 Osteosclerosis [MESH:D010026] (356) 
 Osteopetrosis [MESH:D010022] (318) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Bone Diseases, Endocrine [MESH:D001849] (747) 
 Congenital Hypothyroidism [MESH:D003409] (266) 
 Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)
 Bone Diseases, Metabolic [MESH:D001851] (3492) 
 Osteoporosis [MESH:D010024] (3037) 
 Osteoporosis, Postmenopausal [MESH:D015663] (2351)
 Osteonecrosis [MESH:D010020] (539) 
 Femur Head Necrosis [MESH:D005271] (268)
 Jaw Diseases [MESH:D007571] (1601) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
 Joint Diseases [MESH:D007592] (4657) 
 Synovitis [MESH:D013585] (270)
 Arthritis [MESH:D001168] (4416) 
 Arthritis, Experimental [MESH:D001169] (3142)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Chondrocalcinosis [MESH:D002805] (213)
 Sacroiliitis [MESH:D058566] (202)
 Gout [MESH:D006073] (261) 
 Arthritis, Gouty [MESH:D015210] (211)
 Muscular Diseases [MESH:D009135] (4071) 
 Muscle Weakness [MESH:D018908] (478)
 Musculoskeletal Abnormalities [MESH:D009139] (3796) 
 Craniofacial Abnormalities [MESH:D019465] (3098) 
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
 Rheumatic Diseases [MESH:D012216] (4032) 
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Gout [MESH:D006073] (261) 
 Arthritis, Gouty [MESH:D015210] (211)
C06. Digestive System Diseases 
C06. Digestive System Diseases
 Digestive System Diseases [MESH:D004066] (9461) 
 Pancreatic Diseases [MESH:D010182] (4453)
 Biliary Tract Diseases [MESH:D001660] (3845) 
 Bile Duct Diseases [MESH:D001649] (3512) 
 Cholestasis [MESH:D002779] (3419)
 Digestive System Neoplasms [MESH:D004067] (7493) 
 Gastrointestinal Neoplasms [MESH:D005770] (6460) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Liver Neoplasms [MESH:D008113] (6048) 
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Gastrointestinal Diseases [MESH:D005767] (7443) 
 Esophageal Diseases [MESH:D004935] (4255) 
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Gastrointestinal Neoplasms [MESH:D005770] (6460) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
 Peptic Ulcer [MESH:D010437] (3172) 
 Stomach Ulcer [MESH:D013276] (2915)
 Stomach Diseases [MESH:D013272] (5325) 
 Stomach Neoplasms [MESH:D013274] (4942)
 Peptic Ulcer [MESH:D010437] (2994) 
 Stomach Ulcer [MESH:D013276] (2915)
 Liver Diseases [MESH:D008107] (8167) 
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Fatty Liver [MESH:D005234] (3584)
 Hepatitis [MESH:D006505] (3883)
 Hepatic Insufficiency [MESH:D048550] (2771) 
 Liver Failure [MESH:D017093] (2768) 
 Liver Failure, Acute [MESH:D017114] (2404)
 Liver Cirrhosis [MESH:D008103] (5542) 
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Liver Cirrhosis, Experimental [MESH:D008106] (4589)
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Liver Neoplasms [MESH:D008113] (6048) 
 Carcinoma, Hepatocellular [MESH:D006528] (5375)
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria, Acute Hepatic [MESH:C562618] (99)
C07. Stomatognathic Diseases 
C07. Stomatognathic Diseases
 Stomatognathic Diseases [MESH:D009057] (5348) 
 Jaw Diseases [MESH:D007571] (1608) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
 Mouth Diseases [MESH:D009059] (4783) 
 Behcet Syndrome [MESH:D001528] (1784)
 Facial Paralysis [MESH:D005158] (238)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
C08. Respiratory Tract Diseases 
C08. Respiratory Tract Diseases
 Respiratory Tract Diseases [MESH:D012140] (7881) 
 Bronchial Diseases [MESH:D001982] (4382) 
 Asthma [MESH:D001249] (4098)
 Lung Diseases [MESH:D008171] (7249) 
 Hypertension, Pulmonary [MESH:D006976] (2000)
 Pneumonia [MESH:D011014] (3482)
 Pulmonary Edema [MESH:D011654] (2109)
 Pulmonary Embolism [MESH:D011655] (1118)
 Lung Diseases, Obstructive [MESH:D008173] (4697) 
 Asthma [MESH:D001249] (3903)
 Lung Injury [MESH:D055370] (3688) 
 Acute Lung Injury [MESH:D055371] (1907)
 Lung Neoplasms [MESH:D008175] (6012) 
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
 Respiration Disorders [MESH:D012120] (2218) 
 Apnea [MESH:D001049] (748) 
 Sleep Apnea Syndromes [MESH:D012891] (570)
 Respiratory Hypersensitivity [MESH:D012130] (4401) 
 Asthma [MESH:D001249] (4098)
 Respiratory Tract Infections [MESH:D012141] (3926) 
 Pneumonia [MESH:D011014] (3482)
 Respiratory Tract Neoplasms [MESH:D012142] (6053) 
 Lung Neoplasms [MESH:D008175] (6013) 
 Bronchial Neoplasms [MESH:D001984] (3608) 
 Carcinoma, Bronchogenic [MESH:D002283] (3606) 
 Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
C10. Nervous System Diseases 
C10. Nervous System Diseases
 Z. Exceptions (4027) 
 Not Fully Specified [NFS] (4027)
 Nervous System Diseases [MESH:D009422] (13325) 
 Autonomic Nervous System Diseases [MESH:D001342] (882)
 Restless Legs Syndrome [MESH:D012148] (379)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Myasthenia Gravis [MESH:D009157] (632)
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Central Nervous System Diseases [MESH:D002493] (9745) 
 Brain Diseases [MESH:D001927] (9294) 
 Brain Injuries [MESH:D001930] (3429)
 Basal Ganglia Diseases [MESH:D001480] (4268) 
 Huntington Disease [MESH:D006816] (540)
 Brain Damage, Chronic [MESH:D001925] (311) 
 Cerebral Palsy [MESH:D002547] (300)
 Brain Diseases, Metabolic [MESH:D001928] (3351) 
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Cerebrovascular Disorders [MESH:D002561] (5542) 
 Brain Ischemia [MESH:D002545] (4873) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Arterial Diseases [MESH:D020765] (2463) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873)
 Pituitary Apoplexy [MESH:D010899] (125)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Dementia [MESH:D003704] (4498) 
 Alzheimer Disease [MESH:D000544] (4275)
 Huntington Disease [MESH:D006816] (540)
 Epilepsy [MESH:D004827] (6274) 
 Epilepsies, Myoclonic [MESH:D004831] (1344)
 Seizures [MESH:D012640] (4502)
 Status Epilepticus [MESH:D013226] (4014)
 Epilepsy, Generalized [MESH:D004829] (1431) 
 Epilepsy, Tonic-Clonic [MESH:D004830] (1042)
 Spasms, Infantile [MESH:D013036] (468)
 Hypothalamic Diseases [MESH:D007027] (1833) 
 Pituitary Diseases [MESH:D010900] (1808) 
 Pituitary Apoplexy [MESH:D010899] (125)
 Hyperpituitarism [MESH:D006964] (1250) 
 Pituitary ACTH Hypersecretion [MESH:D047748] (599)
 Movement Disorders [MESH:D009069] (4823) 
 Dyskinesias [MESH:D020820] (1827) 
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Chorea [MESH:D002819] (651) 
 Huntington Disease [MESH:D006816] (540)
 Ocular Motility Disorders [MESH:D015835] (364) 
 Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)
 Spinal Cord Diseases [MESH:D013118] (4376) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Cranial Nerve Diseases [MESH:D003389] (2004) 
 Ocular Motility Disorders [MESH:D015835] (1697) 
 Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)
 Demyelinating Diseases [MESH:D003711] (2917) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Nervous System Malformations [MESH:D009421] (3354) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Spastic Paraplegia, Hereditary [MESH:D015419] (449) 
 Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53)
 Neurodegenerative Diseases [MESH:D019636] (6613) 
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243) 
 Huntington Disease [MESH:D006816] (540)
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Spastic Paraplegia, Hereditary [MESH:D015419] (449) 
 Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53)
 Motor Neuron Disease [MESH:D016472] (3670) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218) 
 Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)
 Tauopathies [MESH:D024801] (4289) 
 Alzheimer Disease [MESH:D000544] (4275)
 TDP-43 Proteinopathies [MESH:D057177] (3337) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Neurologic Manifestations [MESH:D009461] (8964) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Pain [MESH:D010146] (3875)
 Paresis [MESH:D010291] (419)
 Seizures [MESH:D012640] (4514)
 Dyskinesias [MESH:D020820] (3365) 
 Ataxia [MESH:D001259] (1138)
 Catalepsy [MESH:D002375] (1429)
 Hyperkinesis [MESH:D006948] (1799)
 Tremor [MESH:D014202] (840)
 Myoclonus [MESH:D009207] (427) 
 Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)
 Neurobehavioral Manifestations [MESH:D019954] (5230) 
 Psychomotor Disorders [MESH:D011596] (576)
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Fasciculation [MESH:D005207] (204)
 Muscle Weakness [MESH:D018908] (478)
 Spasm [MESH:D013035] (418) 
 Trismus [MESH:D014313] (221)
 Paralysis [MESH:D010243] (2043) 
 Facial Paralysis [MESH:D005158] (238)
 Neuromuscular Diseases [MESH:D009468] (7336) 
 Motor Neuron Disease [MESH:D016472] (3670) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Neuromuscular Junction Diseases [MESH:D020511] (712) 
 Myasthenia Gravis [MESH:D009157] (632)
 Peripheral Nervous System Diseases [MESH:D010523] (6151) 
 Diabetic Neuropathies [MESH:D003929] (2442)
 Polyneuropathies [MESH:D011115] (1134) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Spastic Paraplegia, Hereditary [MESH:D015419] (449) 
 Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53)
 Neurotoxicity Syndromes [MESH:D020258] (4570) 
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912) 
 Lead Poisoning, Nervous System [MESH:D020263] (102)
 Sleep Disorders [MESH:D012893] (2050) 
 Dyssomnias [MESH:D020920] (1417) 
 Sleep Disorders, Intrinsic [MESH:D020919] (1270) 
 Restless Legs Syndrome [MESH:D012148] (379)
 Sleep Apnea Syndromes [MESH:D012891] (570)
 Parasomnias [MESH:D020447] (453) 
 Restless Legs Syndrome [MESH:D012148] (379)
 Trauma, Nervous System [MESH:D020196] (3997) 
 Craniocerebral Trauma [MESH:D006259] (3507) 
 Brain Injuries [MESH:D001930] (3431)
C11. Eye Diseases 
C11. Eye Diseases
 Z. Exceptions (245) 
 Not Fully Specified [NFS] (245)
 Eye Diseases [MESH:D005128] (6245) 
 Eye Manifestations [MESH:D005132] (208) 
 Eye Pain [MESH:D058447] (207)
 Ocular Motility Disorders [MESH:D015835] (1699) 
 Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)
 Retinal Diseases [MESH:D012164] (3747) 
 Retinitis [MESH:D012173] (137)
 Uveal Diseases [MESH:D014603] (2428) 
 Uveitis [MESH:D014605] (2157) 
 Panuveitis [MESH:D015864] (1805) 
 Uveitis, Anterior [MESH:D014606] (1791) 
 Behcet Syndrome [MESH:D001528] (1784)
C12. Male Urogenital Diseases 
C12. Male Urogenital Diseases
 Male Urogenital Diseases [MESH:D052801] (8891) 
 Genital Diseases, Male [MESH:D005832] (6794) 
 Penile Diseases [MESH:D010409] (1805)
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Prostatic Neoplasms [MESH:D011471] (6135)
 Infertility [MESH:D007246] (2909) 
 Infertility, Male [MESH:D007248] (2851)
 Prostatic Diseases [MESH:D011469] (6204) 
 Prostatic Neoplasms [MESH:D011471] (6135)
 Urogenital Neoplasms [MESH:D014565] (6932) 
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Prostatic Neoplasms [MESH:D011471] (6135)
 Urologic Neoplasms [MESH:D014571] (5315) 
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Urologic Diseases [MESH:D014570] (7792) 
 Urinary Tract Infections [MESH:D014552] (984)
 Kidney Diseases [MESH:D007674] (7242) 
 Diabetes Insipidus [MESH:D003919] (354)
 Nephrocalcinosis [MESH:D009397] (311)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758)
 Nephrolithiasis [MESH:D053040] (492) 
 Kidney Calculi [MESH:D007669] (455)
 Renal Insufficiency [MESH:D051437] (4951) 
 Acute Kidney Injury [MESH:D058186] (4142) 
 Kidney Tubular Necrosis, Acute [MESH:D007683] (974)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058) 
 Acidosis, Renal Tubular [MESH:D000141] (225) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Urinary Bladder Diseases [MESH:D001745] (4374) 
 Cystitis [MESH:D003556] (604)
 Urination Disorders [MESH:D014555] (3598) 
 Hematuria [MESH:D006417] (477)
 Oliguria [MESH:D009846] (307)
 Proteinuria [MESH:D011507] (3293)
 Urolithiasis [MESH:D052878] (585) 
 Nephrolithiasis [MESH:D053040] (492) 
 Kidney Calculi [MESH:D007669] (455)
 Urinary Calculi [MESH:D014545] (521) 
 Kidney Calculi [MESH:D007669] (455)
C13. Female Urogenital Diseases and Pregnancy Complications 
C13. Female Urogenital Diseases and Pregnancy Complications
 Female Urogenital Diseases [MESH:D052776] (8724) 
 Genital Diseases, Female [MESH:D005831] (5563) 
 Endometriosis [MESH:D004715] (2461)
 Urogenital Neoplasms [MESH:D014565] (5792) 
 Urologic Neoplasms [MESH:D014571] (5315) 
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Urologic Diseases [MESH:D014570] (7793) 
 Urinary Tract Infections [MESH:D014552] (984)
 Kidney Diseases [MESH:D007674] (7242) 
 Diabetes Insipidus [MESH:D003919] (354)
 Nephrocalcinosis [MESH:D009397] (311)
 Kidney Neoplasms [MESH:D007680] (3966) 
 Carcinoma, Renal Cell [MESH:D002292] (2975)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758)
 Nephrolithiasis [MESH:D053040] (492) 
 Kidney Calculi [MESH:D007669] (455)
 Renal Insufficiency [MESH:D051437] (4951) 
 Acute Kidney Injury [MESH:D058186] (4142) 
 Kidney Tubular Necrosis, Acute [MESH:D007683] (974)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058) 
 Acidosis, Renal Tubular [MESH:D000141] (225) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Urinary Bladder Diseases [MESH:D001745] (4375) 
 Cystitis [MESH:D003556] (604)
 Urination Disorders [MESH:D014555] (3598) 
 Hematuria [MESH:D006417] (477)
 Oliguria [MESH:D009846] (307)
 Proteinuria [MESH:D011507] (3293)
 Urolithiasis [MESH:D052878] (585) 
 Nephrolithiasis [MESH:D053040] (492) 
 Kidney Calculi [MESH:D007669] (455)
 Urinary Calculi [MESH:D014545] (521) 
 Kidney Calculi [MESH:D007669] (455)
 Pregnancy Complications [MESH:D011248] (4768) 
 Prenatal Injuries [MESH:D049188] (1314)
C14. Cardiovascular Diseases 
C14. Cardiovascular Diseases
 Cardiovascular Diseases [MESH:D002318] (10123) 
 Heart Diseases [MESH:D006331] (8614) 
 Cardiomegaly [MESH:D006332] (4081)
 Heart Failure [MESH:D006333] (4058)
 Arrhythmias, Cardiac [MESH:D001145] (4679) 
 Bradycardia [MESH:D001919] (1899)
 Long QT Syndrome [MESH:D008133] (693)
 Tachycardia [MESH:D013610] (3339)
 Arrhythmia, Sinus [MESH:D001146] (324) 
 Sick Sinus Syndrome [MESH:D012804] (293)
 Heart Block [MESH:D006327] (571) 
 Sick Sinus Syndrome [MESH:D012804] (293)
 Cardiomyopathies [MESH:D009202] (5331) 
 Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Heart Valve Diseases [MESH:D006349] (3333) 
 Aortic Valve Stenosis [MESH:D001024] (1742) 
 Aortic Stenosis, Subvalvular [MESH:D001020] (1455) 
 Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)
 Myocardial Ischemia [MESH:D017202] (5787) 
 Myocardial Infarction [MESH:D009203] (4122)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Ventricular Outflow Obstruction [MESH:D014694] (976) 
 Aortic Valve Stenosis [MESH:D001024] (810) 
 Aortic Stenosis, Subvalvular [MESH:D001020] (203)
 Vascular Diseases [MESH:D014652] (8691) 
 Hyperemia [MESH:D006940] (2372)
 Hypertension [MESH:D006973] (5655)
 Hypotension [MESH:D007022] (4045)
 Cerebrovascular Disorders [MESH:D002561] (5541) 
 Brain Ischemia [MESH:D002545] (4873) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Arterial Diseases [MESH:D020765] (2468) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873)
 Pituitary Apoplexy [MESH:D010899] (125)
 Stroke [MESH:D020521] (3702) 
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Embolism and Thrombosis [MESH:D016769] (3374) 
 Embolism [MESH:D004617] (1137) 
 Pulmonary Embolism [MESH:D011655] (1118)
 Myocardial Ischemia [MESH:D017202] (5791) 
 Myocardial Infarction [MESH:D009203] (4151)
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Vasculitis [MESH:D014657] (2604) 
 Behcet Syndrome [MESH:D001528] (1784)
C15. Hemic and Lymphatic Diseases 
C15. Hemic and Lymphatic Diseases
 Lymphatic Diseases [MESH:D008206] (5167) 
 Lymphoproliferative Disorders [MESH:D008232] (4638) 
 Lymphoma [MESH:D008223] (3684) 
 Lymphoma, Non-Hodgkin [MESH:D008228] (3330) 
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities 
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
 Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152) 
 Congenital Abnormalities [MESH:D000013] (8109) 
 Abnormalities, Drug-Induced [MESH:D000014] (1024)
 Abnormalities, Multiple [MESH:D000015] (3192) 
 Bamforth syndrome [MESH:C537901] (186)
 Cardiovascular Abnormalities [MESH:D018376] (3294) 
 Heart Defects, Congenital [MESH:D006330] (2611) 
 Long QT Syndrome [MESH:D008133] (693)
 Musculoskeletal Abnormalities [MESH:D009139] (3779) 
 Craniofacial Abnormalities [MESH:D019465] (3064) 
 Maxillofacial Abnormalities [MESH:D019767] (1448) 
 Jaw Abnormalities [MESH:D007569] (1435) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
 Nervous System Malformations [MESH:D009421] (3354) 
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Spastic Paraplegia, Hereditary [MESH:D015419] (449) 
 Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53)
 Stomatognathic System Abnormalities [MESH:D018640] (1705) 
 Maxillofacial Abnormalities [MESH:D019767] (1447) 
 Jaw Abnormalities [MESH:D007569] (1438) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
 Mouth Abnormalities [MESH:D009056] (1383) 
 Cleft Palate [MESH:D002972] (1330) 
 Bamforth syndrome [MESH:C537901] (186)
 Genetic Diseases, Inborn [MESH:D030342] (9766) 
 ACTH Deficiency, Isolated [MESH:C562707] (124)
 Dwarfism [MESH:D004392] (783) 
 Congenital Hypothyroidism [MESH:D003409] (266) 
 Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)
 Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465) 
 Huntington Disease [MESH:D006816] (540)
 Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899) 
 Charcot-Marie-Tooth Disease [MESH:D002607] (627) 
 Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)
 Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)
 Spastic Paraplegia, Hereditary [MESH:D015419] (449) 
 Spastic Paraplegia 39, Autosomal Recessive [MESH:C567433] (53)
 Metabolism, Inborn Errors [MESH:D008661] (6032) 
 Butyrylcholinesterase deficiency [MESH:C537417] (176)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Peroxisomal Disorders [MESH:D018901] (1788) 
 Acatalasia [MESH:D020642] (788)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria, Acute Hepatic [MESH:C562618] (99)
 Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496) 
 Gout [MESH:D006073] (261) 
 Arthritis, Gouty [MESH:D015210] (211)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027) 
 Acidosis, Renal Tubular [MESH:D000141] (225) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Skin Diseases, Genetic [MESH:D012873] (3456) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria, Acute Hepatic [MESH:C562618] (99)
 Infant, Newborn, Diseases [MESH:D007232] (3064) 
 Asphyxia Neonatorum [MESH:D001238] (1648)
C17. Skin and Connective Tissue Diseases 
C17. Skin and Connective Tissue Diseases
 Connective Tissue Diseases [MESH:D003240] (4490) 
 Rheumatic Diseases [MESH:D012216] (3619) 
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Skin Diseases [MESH:D012871] (8774) 
 Keratosis [MESH:D007642] (1941)
 Breast Diseases [MESH:D001941] (6148) 
 Breast Neoplasms [MESH:D001943] (6077)
 Hair Diseases [MESH:D006201] (1891) 
 Bamforth syndrome [MESH:C537901] (186)
 Hirsutism [MESH:D006628] (323)
 Hypotrichosis [MESH:D007039] (1513) 
 Alopecia [MESH:D000505] (1453)
 Skin Diseases, Genetic [MESH:D012873] (3481) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria, Acute Hepatic [MESH:C562618] (99)
 Skin Diseases, Metabolic [MESH:D012875] (1574) 
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria, Acute Hepatic [MESH:C562618] (99)
 Skin Diseases, Papulosquamous [MESH:D017444] (3392) 
 Psoriasis [MESH:D011565] (3278)
 Skin Diseases, Vascular [MESH:D017445] (3288) 
 Behcet Syndrome [MESH:D001528] (1784)
C18. Nutritional and Metabolic Diseases 
C18. Nutritional and Metabolic Diseases
 Metabolic Diseases [MESH:D008659] (9025) 
 Acid-Base Imbalance [MESH:D000137] (854) 
 Acidosis [MESH:D000138] (626) 
 Acidosis, Renal Tubular [MESH:D000141] (225) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Brain Diseases, Metabolic [MESH:D001928] (3350) 
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Calcium Metabolism Disorders [MESH:D002128] (3634) 
 Hypocalcemia [MESH:D006996] (378)
 Calcinosis [MESH:D002114] (2989) 
 Nephrocalcinosis [MESH:D009397] (311)
 Glucose Metabolism Disorders [MESH:D044882] (6122) 
 Diabetes Mellitus [MESH:D003920] (5891) 
 Diabetes Mellitus, Experimental [MESH:D003921] (4771)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
 Diabetes Mellitus, Type 2 [MESH:D003924] (4219)
 Hypoglycemia [MESH:D007003] (2420) 
 ACTH Deficiency, Isolated [MESH:C562707] (124)
 Metabolism, Inborn Errors [MESH:D008661] (6028) 
 Butyrylcholinesterase deficiency [MESH:C537417] (176)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Peroxisomal Disorders [MESH:D018901] (1788) 
 Acatalasia [MESH:D020642] (788)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria, Acute Hepatic [MESH:C562618] (99)
 Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496) 
 Gout [MESH:D006073] (261) 
 Arthritis, Gouty [MESH:D015210] (211)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026) 
 Acidosis, Renal Tubular [MESH:D000141] (225) 
 Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria, Acute Hepatic [MESH:C562618] (99)
 Proteostasis Deficiencies [MESH:D057165] (3522) 
 TDP-43 Proteinopathies [MESH:D057177] (3337) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Skin Diseases, Metabolic [MESH:D012875] (1574) 
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria, Acute Hepatic [MESH:C562618] (99)
 Water-Electrolyte Imbalance [MESH:D014883] (2790) 
 Hypernatremia [MESH:D006955] (215)
 Hypocalcemia [MESH:D006996] (368)
 Hypokalemia [MESH:D007008] (1041)
 Nutrition Disorders [MESH:D009748] (4945) 
 Malnutrition [MESH:D044342] (2754) 
 Deficiency Diseases [MESH:D003677] (2742) 
 Protein Deficiency [MESH:D011488] (1057)
 Overnutrition [MESH:D044343] (4463) 
 Obesity [MESH:D009765] (4462) 
 Proopiomelanocortin Deficiency [MESH:C565726] (200)
C19. Endocrine System Diseases 
C19. Endocrine System Diseases
 Endocrine System Diseases [MESH:D004700] (8062) 
 ACTH Deficiency, Isolated [MESH:C562707] (124)
 Adrenal Gland Diseases [MESH:D000307] (2397) 
 Adrenal Cortex Diseases [MESH:D000303] (969)
 Adrenal Insufficiency [MESH:D000309] (1599) 
 Proopiomelanocortin Deficiency [MESH:C565726] (200)
 Adrenocortical Hyperfunction [MESH:D000308] (618) 
 Cushing Syndrome [MESH:D003480] (282)
 Diabetes Mellitus [MESH:D003920] (6159) 
 Diabetes Mellitus, Experimental [MESH:D003921] (4771)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
 Diabetes Mellitus, Type 2 [MESH:D003924] (4219)
 Diabetes Complications [MESH:D048909] (4129) 
 Diabetic Neuropathies [MESH:D003929] (2443)
 Dwarfism [MESH:D004392] (698) 
 Congenital Hypothyroidism [MESH:D003409] (266) 
 Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)
 Gonadal Disorders [MESH:D006058] (5088) 
 Puberty, Delayed [MESH:D011628] (449)
 Pituitary Diseases [MESH:D010900] (1829) 
 Diabetes Insipidus [MESH:D003919] (302)
 Pituitary Apoplexy [MESH:D010899] (125)
 Hyperpituitarism [MESH:D006964] (1259) 
 Pituitary ACTH Hypersecretion [MESH:D047748] (599)
 Thyroid Diseases [MESH:D013959] (2808) 
 Hypothyroidism [MESH:D007037] (496) 
 Bamforth syndrome [MESH:C537901] (186)
 Congenital Hypothyroidism [MESH:D003409] (266) 
 Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)
C20. Immune System Diseases 
C20. Immune System Diseases
 Z. Exceptions (350) 
 Not Fully Specified [NFS] (350)
 Immune System Diseases [MESH:D007154] (7674) 
 Autoimmune Diseases [MESH:D001327] (5067) 
 Arthritis, Rheumatoid [MESH:D001172] (3601)
 Diabetes Mellitus, Type 1 [MESH:D003922] (1893)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Myasthenia Gravis [MESH:D009157] (632)
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Hypersensitivity [MESH:D006967] (5873) 
 Hypersensitivity, Immediate [MESH:D006969] (4980) 
 Respiratory Hypersensitivity [MESH:D012130] (4250) 
 Asthma [MESH:D001249] (3914)
 Immunoproliferative Disorders [MESH:D007160] (4761) 
 Lymphoproliferative Disorders [MESH:D008232] (4734) 
 Lymphoma [MESH:D008223] (3684) 
 Lymphoma, Non-Hodgkin [MESH:D008228] (3330) 
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
C23. Pathological Conditions, Signs and Symptoms 
C23. Pathological Conditions, Signs and Symptoms
 Pathological Conditions, Anatomical [MESH:D020763] (6074) 
 Alopecia [MESH:D000505] (1383)
 Calculi [MESH:D002137] (756) 
 Urinary Calculi [MESH:D014545] (521) 
 Kidney Calculi [MESH:D007669] (455)
 Hypertrophy [MESH:D006984] (4476) 
 Cardiomegaly [MESH:D006332] (3802)
 Pathologic Processes [MESH:D010335] (9863) 
 Muscle Weakness [MESH:D018908] (478)
 Arrhythmias, Cardiac [MESH:D001145] (4658) 
 Bradycardia [MESH:D001919] (1899)
 Long QT Syndrome [MESH:D008133] (691)
 Tachycardia [MESH:D013610] (3339)
 Arrhythmia, Sinus [MESH:D001146] (324) 
 Sick Sinus Syndrome [MESH:D012804] (293)
 Heart Block [MESH:D006327] (571) 
 Sick Sinus Syndrome [MESH:D012804] (293)
 Death [MESH:D003643] (1328) 
 Death, Sudden [MESH:D003645] (725) 
 Sudden Infant Death [MESH:D013398] (268)
 Disease Attributes [MESH:D020969] (3654) 
 Disease Progression [MESH:D018450] (2868)
 Recurrence [MESH:D012008] (830)
 Disease Susceptibility [MESH:D004198] (1200) 
 Genetic Predisposition to Disease [MESH:D020022] (966)
 Hemorrhage [MESH:D006470] (4451) 
 Hematuria [MESH:D006417] (477)
 Intracranial Hemorrhages [MESH:D020300] (3241) 
 Cerebral Hemorrhage [MESH:D002543] (2872)
 Inflammation [MESH:D007249] (5241) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Necrosis [MESH:D009336] (4019) 
 Osteonecrosis [MESH:D010020] (537) 
 Femur Head Necrosis [MESH:D005271] (266)
 Neoplastic Processes [MESH:D009385] (5317) 
 Neoplasm Invasiveness [MESH:D009361] (3388)
 Neoplasm Metastasis [MESH:D009362] (4441)
 Carcinogenesis [MESH:D063646] (3391) 
 Cell Transformation, Neoplastic [MESH:D002471] (3389)
 Postoperative Complications [MESH:D011183] (5311) 
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Signs and Symptoms [MESH:D012816] (10659) 
 Edema [MESH:D004487] (3726)
 Body Temperature Changes [MESH:D001832] (3130) 
 Fever [MESH:D005334] (2856)
 Hypothermia [MESH:D007035] (2075)
 Body Weight [MESH:D001835] (4972) 
 Body Weight Changes [MESH:D001836] (3206) 
 Weight Gain [MESH:D015430] (2595)
 Weight Loss [MESH:D015431] (2512)
 Overweight [MESH:D050177] (4455) 
 Obesity [MESH:D009765] (4454) 
 Proopiomelanocortin Deficiency [MESH:C565726] (200)
 Eye Manifestations [MESH:D005132] (213) 
 Eye Pain [MESH:D058447] (207)
 Neurologic Manifestations [MESH:D009461] (8702) 
 Pain [MESH:D010146] (3869)
 Paresis [MESH:D010291] (419)
 Seizures [MESH:D012640] (4502)
 Sleep Disorders [MESH:D012893] (1301)
 Dyskinesias [MESH:D020820] (3285) 
 Ataxia [MESH:D001259] (984)
 Catalepsy [MESH:D002375] (1429)
 Hyperkinesis [MESH:D006948] (1799)
 Tremor [MESH:D014202] (840)
 Neurobehavioral Manifestations [MESH:D019954] (4706) 
 Psychomotor Disorders [MESH:D011596] (576)
 Communication Disorders [MESH:D003147] (2918) 
 Learning Disorders [MESH:D007859] (2727)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Fasciculation [MESH:D005207] (204)
 Muscle Weakness [MESH:D018908] (478)
 Spasm [MESH:D013035] (418) 
 Trismus [MESH:D014313] (221)
 Paralysis [MESH:D010243] (2298) 
 Facial Paralysis [MESH:D005158] (238)
 Pain [MESH:D010146] (4511) 
 Chest Pain [MESH:D002637] (2642)
 Eye Pain [MESH:D058447] (207)
 Signs and Symptoms, Digestive [MESH:D012817] (3095) 
 Anorexia [MESH:D000855] (854)
 Constipation [MESH:D003248] (506)
 Nausea [MESH:D009325] (2300)
 Signs and Symptoms, Respiratory [MESH:D012818] (2724) 
 Anoxia [MESH:D000860] (1698)
 Apnea [MESH:D001049] (415)
 Urological Manifestations [MESH:D020924] (3532) 
 Hypercalciuria [MESH:D053565] (330)
 Oliguria [MESH:D009846] (307)
 Proteinuria [MESH:D011507] (3293)
 Virilism [MESH:D014770] (327) 
 Hirsutism [MESH:D006628] (323)
C25. Chemically-Induced Disorders 
C25. Chemically-Induced Disorders
 Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839) 
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Poisoning [MESH:D011041] (6703) 
 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 [MESH:D007855] (515) 
 Lead Poisoning, Nervous System [MESH:D020263] (102)
 Neurotoxicity Syndromes [MESH:D020258] (3323) 
 Dyskinesia, Drug-Induced [MESH:D004409] (1389)
 Substance-Related Disorders [MESH:D019966] (6308) 
 Amphetamine-Related Disorders [MESH:D019969] (2858)
 Cocaine-Related Disorders [MESH:D019970] (3054)
 Psychoses, Substance-Induced [MESH:D011605] (2052)
 Substance Withdrawal Syndrome [MESH:D013375] (2956)
 Alcohol-Related Disorders [MESH:D019973] (3869) 
 Alcoholism [MESH:D000437] (1519)
 Alcohol-Induced Disorders [MESH:D020751] (3350) 
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Opioid-Related Disorders [MESH:D009293] (1491) 
 Heroin Dependence [MESH:D006556] (950)
C26. Wounds and Injuries 
C26. Wounds and Injuries
 Wounds and Injuries [MESH:D014947] (5171) 
 Burns [MESH:D002056] (2565)
 Craniocerebral Trauma [MESH:D006259] (3523) 
 Brain Injuries [MESH:D001930] (3431)
 Trauma, Nervous System [MESH:D020196] (3535) 
 Craniocerebral Trauma [MESH:D006259] (3507) 
 Brain Injuries [MESH:D001930] (3431)
D02. Organic Chemicals 
D02. Organic Chemicals
 Organic Chemicals [MESH:D009930] (75987) 
 Organophosphorus Compounds [MESH:D009943] (2593) 
 Organothiophosphorus Compounds [MESH:D009946] (291)
 Sulfur Compounds [MESH:D013457] (10450) 
 Organothiophosphorus Compounds [MESH:D009946] (291)
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment 
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment
 Diagnosis [MESH:D003933] (1924) 
 Diagnostic Techniques and Procedures [MESH:D019937] (1902) 
 Physical Examination [MESH:D010808] (1041) 
 Body Constitution [MESH:D001824] (450) 
 Body Weights and Measures [MESH:D001837] (448) 
 Body Size [MESH:D049628] (439) 
 Body Weight [MESH:D001835] (433) 
 Overweight [MESH:D050177] (428) 
 Obesity [MESH:D009765] (427) 
 Proopiomelanocortin Deficiency [MESH:C565726] (200)
G. Phenomena and Processes 
G. Phenomena and Processes
 Physiological Phenomena [MESH:D010829] (788) 
 Body Constitution [MESH:D001824] (453) 
 Body Weights and Measures [MESH:D001837] (444) 
 Body Size [MESH:D049628] (438) 
 Body Weight [MESH:D001835] (433) 
 Overweight [MESH:D050177] (428) 
 Obesity [MESH:D009765] (427) 
 Proopiomelanocortin Deficiency [MESH:C565726] (200)