|
411
|
|
|
Monoamine oxidase A |
BRNRS, MAO-A |
Akinetic-rigid variant of huntington disease, Antisocial personality disorder, Autism, Behavior disorders, Bipolar disorder, Breast cancer, Brugada syndrome, Cognitive disorder, Disorder of fetal nutrition, Dysthymic disorder, End stage liver disease, Endometrioma, Endometriosis, Extra-adrenal pheochromocytoma, Fulminant hepatic failure with cerebral edema, Hepatic coma, Hepatic encephalopathy, Hepatic stupor, Huntington disease, Impaired cognition, Liver failure, Mental disorders, Mental depression, Mental depression with psychotic features, Mental retardation, Brunner syndrome, Mood disorder, Myopathy, Parkinson disease, Pheochromocytoma, Poor fetal nutrition, Psychosis, SchizophreniaView all (18 more) |
|
412
|
|
|
Monoamine oxidase B |
- |
Akinetic-rigid variant of huntington disease, Alzheimer disease, Anemia, Autism, Bipolar disorder, Colonic neoplasms, Endometrioma, Endometriosis, Extra-adrenal pheochromocytoma, Fulminant hepatic failure with cerebral edema, Hepatic coma, Hepatic encephalopathy, Hepatic stupor, Huntington disease, Mental depression, Mood disorder, Parkinson disease, Pheochromocytoma, Schizophrenia, Senile dementia, Senile plaquesView all (6 more) |
|
413
|
|
|
Microtubule associated protein 1B |
DFNA83, FUTSCH, MAP5, PPP1R102, PVNH9 |
|
|
414
|
|
|
Microtubule associated protein 2 |
MAP-2, MAP2A, MAP2B, MAP2C |
Arthritis, Bipolar disorder, Colorectal cancer, Juvenile arthritis, Lewy body disease, Mental depression, Miscarriage, Mood disorder, Parkinson disease, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease |
|
415
|
|
|
Microtubule associated protein 4 |
- |
|
|
416
|
|
|
Microtubule associated protein 6 |
MAP6-N, MTAP6, N-STOP, STOP |
|
|
417
|
|
|
Microtubule associated protein tau |
DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1, MTBT2, PPND, PPP1R103, TAU, Tau-PHF6, tau-40 |
Abulia, Acquired kyphoscoliosis, Akinesia, Alexia, Alopecia, Alopecia, male pattern, Alzheimer disease, Amyotrophic lateral sclerosis, Androgenetic alopecia, Anomia, Anxiety disorder, Aphasia, Apraxia, Arthritis, Atrial fibrillation, Behavioral variant of frontotemporal dementia, Blepharospasm, Brain atrophy, Breast carcinoma, Broca aphasia, Cardiomyopathy, Cerebral atrophy, Cognitive disorder, Compulsive hoarding, Congenital kyphoscoliosis, Degenerative diseases, central nervous system, Dementia, Dementia of frontal lobe, Development disorder, Diabetes mellitus, Dysarthria, Dyscalculia, Dysgraphia, Dyslexia, Dysphagia, Dysphasia, Dyssomnia, Focal dystonia, Frontotemporal cerebral atrophy, Frontotemporal dementia, Grammar-specific speech disorder, Language disorders, Learning disorders, Limb apraxia, Liver carcinoma, Lung diseases, Memory disorders, Age-related memory disorders, Mental depression, Mood disorder, Myocardial diseases, Neurodegenerative disorders, Neuromuscular dysphagia, Oculomotor apraxia, Oculovestibuloauditory syndrome, Osteoarthritis of hip, Parkinson disease, Parkinsonian disease, Paroxysmal atrial fibrillation, Pica, Biliary cirrhosis, Nonfluent aphasia, Progressive non-fluent aphasia, Progressive supranuclear ophthalmoplegia, Progressive supranuclear palsy, Psychosis, Ramsay hunt paralysis syndrome, Respiratory failure, Retrocollis, Seizure, Semantic dementia, Senile dementia, Senile paranoid dementia, Senile plaques, Sleep disorders, Speech disorders, Stereotyped behavior, Supranuclear gaze palsy, Supranuclear palsy, Supranuclear palsy-corticobasal syndrome, Supranuclear palsy-parkinsonism syndrome, Supranuclear palsy-progressive non-fluent aphasia syndrome, Supranuclear palsy-pure akinesia with gait freezing syndrome, Tauopathies, Temporal cortical atrophyView all (70 more) |
|
418
|
|
|
Microtubule affinity regulating kinase 1 |
MARK, Par-1c, Par1c |
|
|
419
|
|
|
Microtubule affinity regulating kinase 3 |
CTAK1, KP78, PAR1A, Par-1a, VIPB |
|
|
420
|
|
|
Methionyl-tRNA synthetase 1 |
CMT2U, ILFS2, ILLD, MARS, METRS, MRS, MTRNS, SPG70, TTD9 |
Alveolar proteinosis, Anemia, Charcot-marie-tooth disease, Developmental delay, Fatty liver, Hypothyroidism, Interstitial lung and liver disease, Lung diseases, Mental retardation, Nephrotic syndrome, Nervous system diseases, Peripheral axonal neuropathy, Spastic paraplegia |
