|
521
|
|
|
MPL proto-oncogene, thrombopoietin receptor |
C-MPL, CD110, MPLV, THCYT2, THPOR, TPOR |
Amegakaryocytic thrombocytopenia, Anemia, Anorexia, Budd-chiari syndrome, Congenital amegakaryocytic thrombocytopenia, Defect of skull ossification, Dwarfism, Dysarthria, Heart septal defects, Hemangioma, Hematologic neoplasms, Hereditary isolated aplastic anemia, Hypertension, Leukemia, Medulloblastoma, Medullomyoblastoma, Melanocytic nevus, Myelodysplasia, Myelodysplastic syndrome, Myelofibrosis, Myeloid leukemia, Myeloproliferative disorder, Myocardial infarction, Pancytopenia, Peripheral arterial stenosis, Polycythemia vera, Portal hypertension, Portal vein thrombosis, Pulmonary arterial hypertension, Scoliosis, Stroke, Thrombocythemia, Thrombocytosis, Transient ischemic attackView all (19 more) |
|
522
|
|
|
Myeloperoxidase |
- |
Alcoholic liver cirrhosis, Alzheimer disease, Urinary bladder cancer, Bladder neoplasm, Cardiovascular diseases, Cerebral ischemia, Cholestasis, Colitis, Colorectal cancer, Dementia, Epileptic encephalopathy, Involutional depression, Involutional paraphrenia, Keratoma, Keratosis, Keratosis blennorrhagica, Kidney disease, Kidney failure, Liver carcinoma, Lung neoplasms, Lung cancer, Lung diseases, Mental depression, Myeloperoxidase deficiency, Pancreatitis, Parkinson disease, Prostatic neoplasms, Prostate cancer, Psychosis, Acute kidney insufficiency, Rheumatoid arthritis, Senile dementia, Ulcerative colitis, UrticariaView all (19 more) |
|
523
|
|
|
MAGUK p55 scaffold protein 1 |
AAG12, DXS552E, EMP55, MRG1, PEMP |
|
|
524
|
|
|
Mercaptopyruvate sulfurtransferase |
MST, TST2, TUM1 |
|
|
525
|
|
|
Mitochondrial inner membrane protein MPV17 |
CMT2EE, MTDPS6, SYM1 |
Cholestasis, Cirrhosis, Cochlear diseases, Developmental delay, Distal amyotrophy, Distal lower limb amyotrophy, Dwarfism, Erosion of cornea, Glomerular hyalinosis, Glomerulosclerosis, Gout, Gouty arthritis, Hypoglycemia, Incontinentia pigmenti achromians, Liver failure, Mitochondrial diseases, Mitochondrial electron transport chain deficiencies, Mitochondrial respiratory chain deficiencies, Navajo familial neurogenic arthropathy, Navajo neurohepatopathy, Nystagmus, Oxidative phosphorylation deficiency, Peripheral axonal neuropathy, Pigmentation disorders, Ptosis, Scoliosis, Sensorimotor neuropathy, Sensory neuropathyView all (13 more) |
|
526
|
|
|
Myelin protein zero |
CHM, CHN2, CMT1, CMT1B, CMT2I, CMT2J, CMT4E, CMTDI3, CMTDID, DSS, HMSNIB, MPP, P0 |
Acquired kyphoscoliosis, Charcot-marie-tooth disease, Congenital hypomyelinating neuropathy, Congenital kyphoscoliosis, Congenital pes cavus, Dejerine-sottas disease, Distal amyotrophy, Distal lower limb amyotrophy, Dysautonomia, Dysmorphic features, Dysphagia, Hearing loss, Hereditary motor and sensory neuropathy, Keratoderma palmoplantar spastic paralysis, Motor and sensory neuropathy, Motor delay, Movement disorders, Nervous system diseases, Neuropathy, Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome, Peripheral axonal neuropathy, Roussy-levy syndrome, Scoliosis, Sensorimotor neuropathy, Sensory neuropathyView all (10 more) |
|
527
|
|
|
Mannose receptor C-type 1 |
CD206, CLEC13D, CLEC13DL, MMR, MRC1L1, bA541I19.1, hMR |
|
|
528
|
|
|
MRE11 double strand break repair nuclease |
ATLD, HNGS1, MRE11A, MRE11B |
Ataxia-oculomotor apraxia, Ataxia-telangiectasia-like disorder, Breast cancer, Breast carcinoma, Hereditary cancer syndrome, Cerebellar ataxia, Cerebellar atrophy, Distal amyotrophy, Dwarfism, Dysarthria, Dysphagia, Esotropia, Hereditary breast and ovarian cancer syndrome, Hyperopia, Hypogonadism, Orofacial dyskinesia, Malignant neoplasm, Melanoma, Nijmegen breakage syndrome-like disorder, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Ovarian neoplasm, Ovarian cancer, Pancreatic neoplasm, Peritoneal carcinoma, Prostate cancer, Scoliosis, Sensorimotor neuropathy, Specific learning disorder, Triple negative breast neoplasms, Tumor predisposition syndrome, Vertical nystagmusView all (18 more) |
|
529
|
|
|
Mitochondrial contact site and cristae organizing system subunit 10 |
C1orf151, MINOS1, MIO10, Mic10 |
|
|
530
|
|
|
Myocardial infarction associated transcript |
C22orf35, GOMAFU, LINC00066, NCRNA00066, RNCR2, lncRNA-MIAT |
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