8271
|
|
|
Myosin heavy chain 2 |
CMYO6, CMYP6, IBM3, MYH2A, MYHSA2, MYHas8, MYPOP, MyHC-2A, MyHC-IIa |
|
8272
|
|
|
Myosin heavy chain 3 |
CPSFS1A, CPSFS1B, CPSKF1A, CPSKF1B, DA2A, DA2B, DA2B3, DA8, HEMHC, MYHC-EMB, MYHSE1, SMHCE |
Arthrogryposis, Arthrogryposis multiplex congenita, Distal arthrogryposis, Contractures, pterygia, and spondylocarpotarsal fusion syndrome, Contractures, pterygia, and variable skeletal fusions syndrome, Desbuquois syndrome, Digitotalar dysmorphism, Meniere disease, Sheldon-hall syndrome |
8273
|
|
|
Myosin heavy chain 6 |
ASD3, CMD1EE, CMH14, MYHC, MYHCA, SSS3, alpha-MHC |
Atrioventricular excitation abnormality, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Atrial flutter, Atrial septal defect, Cardiac arrest, Cardiac arrhythmia, Cardiac conduction disease, Cardiomegaly, Cardiomyopathy, Dilated cardiomyopathy, Conduction disorder of the heart, Congenital heart defects, Congestive heart failure, Sick sinus syndrome, Congenital heart defect, Heart disease, Heart failure, Congenital heart septal defect, Hypertrophic cardiomyopathy, Hypoplastic left heart syndrome, Keppen-lubinsky syndrome, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Migraine, Restrictive cardiomyopathy, Tetralogy of fallot, Ventricular dysfunction, Ventricular fibrillation, Ventricular remodeling, Wolff-parkinson-white syndromeView all (17 more) |
8274
|
|
|
Myosin heavy chain 7 |
CMD1S, CMH1, CMYO7A, CMYO7B, CMYP7A, CMYP7B, MPD1, MYHCB, SPMD, SPMM |
Arrhythmogenic right ventricular cardiomyopathy, Asymmetric septal hypertrophy, Atrial fibrillation, Myosin storage myopathy, Biventricular noncompaction cardiomyopathy, Camptocormia, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Multiminicore myopathy, Conduction disorder of the heart, Congenital epicanthus, Congenital fiber type disproportion myopathy, Congenital heart defects, Congenital heart disease, Congenital myopathy, Coronary stenosis, Distal muscular dystrophy, Distal myopathy, Ebstein anomaly, Hypertrophic cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Gross motor development delay, Heart failure, Hypertension, Hypoplastic left heart syndrome, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Myocardial infarction, Myopathy, Neuromuscular disease, Parieto-occipital craniosynostosis, Pericarditis, Restrictive cardiomyopathy, Craniosynostosis, Scapuloperoneal myopathy, Tetralogy of fallot, Polymorphic ventricular tachycardia, Wolff-parkinson-white syndromeView all (25 more) |
8275
|
|
|
Myosin heavy chain 7B |
MHC14, MYH14, lncMYH7b |
|
8276
|
|
|
Myosin heavy chain 8 |
DA7, MyHC-peri, MyHC-pn, gtMHC-F |
|
8277
|
|
|
Myosin heavy chain 9 |
BDPLT6, DFNA17, EPSTS, FTNS, MATINS, MHA, NMHC-II-A, NMMHC-IIA, NMMHCA |
Isolated sensorineural deafness, Nonsyndromic hearing loss, Breast neoplasms, Basal cell carcinoma, Lobular carcinoma, Congenital cataract, Kidney disease, Obstructive pulmonary disease, Deafness, Autosomal dominant sensorineural deafness, Diabetes mellitus type 1, Diabetic neuropathy, Focal glomerulosclerosis, Glomerulonephritis, Hearing impairment, Hereditary hearing loss, Renal hypertension, Hypertension, Hypertensive nephropathy, Kidney failure, Meniere disease, Nephrotic syndrome, Obesity, Orofacial cleft, Sebastian syndrome, Hearing loss, Thrombocytopenia, Uterine fibroidView all (13 more) |
8278
|
|
|
Myosin light chain 1 |
CMYO14, CMYP14, MLC-1, MLC1, MLC1/3, MLC1F, MLC3F, MYOFTA |
|
8279
|
|
|
Myosin light chain 10 |
MYLC2PL, PLRLC |
Alzheimer disease, Androgenetic alopecia, Angioedema, Basal cell carcinoma, Primary adrenal insufficiency, Glucocorticoid deficiency, Gout, Keratinocyte carcinoma, Major depressive disorder, Non-melanoma skin carcinoma, Skin cancer, Skin disease, Skin neoplasms |
8280
|
|
|
Myosin light chain 11 |
DA1C, HUMMLC2B, MLC2B, MRLC2, MYLPF |
|
