|
621
|
|
|
Myosin light chain 3 |
CMH8, MLC-lV/sb, MLC1SB, MLC1V, VLC1, VLCl |
|
|
622
|
|
|
Myosin light chain 4 |
ALC1, AMLC, GT1, PRO1957 |
|
|
623
|
|
|
Myosin light chain kinase |
AAT7, KRP, MLCK, MLCK1, MLCK108, MLCK210, MMIHS, MMIHS1, MSTP083, MYLK-L, MYLK1, smMLCK |
Aortic aneurysm, Aortic dissection, Aortic valve insufficiency, Arachnodactyly, Berdon syndrome, Bicuspid aortic valve, Cardiac neoplasms, Congenital aneurysm of ascending aorta, Congenital exomphalos, Congenital malrotation of intestine, Congenital omphalocele, Coronary arteriosclerosis, Cryptorchidism, Cutis marmorata, Descending aortic dissection, Dyspnea, paroxysmal, Fetal megacystis, Functional gastrointestinal disorders, Gastrointestinal diseases, Glaucoma, Glioma, Hypercholesterolemia, Hypertension, Ischemic stroke, Megacystis-microcolon-intestinal hypoperistalsis syndrome, Microcolon, Multicystic renal dysplasia, Ovarian adenocarcinoma, Patent ductus arteriosus, Peripheral arterial stenosis, Scoliosis, Subarachnoid hemorrhage, Thoracic aortic aneurysm and aortic dissection, Transient ischemic attack, Vascular diseases, Visceral myopathyView all (21 more) |
|
624
|
|
|
Myosin IA |
BBMI, DFNA48, DIAR15, MIHC, MYHL |
|
|
625
|
|
|
Myosin IC |
MMI-beta, MMIb, MyoIC, NMI, myr2 |
|
|
626
|
|
|
Myosin ID |
PPP1R108, myr4 |
|
|
627
|
|
|
Myosin IE |
FSGS6, HuncM-IC, MYO1C |
|
|
628
|
|
|
Myosin VA |
GS1, MYH12, MYO5, MYR12 |
Acrocephalopolydactyly, Cerebellar cortical atrophy, Cerebellar hypoplasia, Cerebral cortical hemiatrophy, Developmental delay, Elejalde disease, Griscelli syndrome, Hyperlipidemia, Hypopigmentation disorder, Hypopigmentation-immunodeficiency disease, Age-related macular degeneration, Mental retardation, Movement disorders, Myopia, Nervous system diseases, Neuroectodermal melanolysosomal disease, Nystagmus, Optic atrophy, Piebaldism, Retinal diseases, Specific learning disorder, Strabismus, Subcortical cerebral atrophyView all (8 more) |
|
629
|
|
|
Myosin VB |
DIAR2, MVID1, PFIC10 |
Bipolar disorder, Cholestasis, Developmental delay, Hyperchloremia, Inborn errors of metabolism, Intestinal diseases, Intrahepatic cholestasis, Liver neoplasms, Liver cancer, Malnutrition, Microvillus inclusion disease, Myopia, Nephrocalcinosis, Schizophrenia |
|
630
|
|
|
Myosin VI |
DFNA22, DFNB37 |
Deafness, Deafness with hypertrophic cardioyopathy, Deafness, sensorineural, with hypertrophic cardiomyopathy, Hypertension, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome, Prostate cancer, Sensorineural hearing loss |
