4251
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Myosin heavy chain 4 |
MYH2B, MyHC-2B, MyHC-IIb |
Curated: N/A
Unreviewed: Anemia, Colonic neoplasm, Fanconi Anemia, Friedreich Ataxia
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4252
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|
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Myosin heavy chain 6 |
ASD3, CMD1EE, CMH14, MYHC, MYHCA, SSS3, alpha-MHC |
Curated: 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, 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 syndrome, MYH-6 related congenital heart defects, dilated cardiomyopathy 1EE
Unreviewed: Amyotrophic Lateral Sclerosis, Aortic Coarctation, Atrial Fibrillation, Atrial Septal Defect, Atrophy, Autism, Autism Spectrum Disorder, Bicuspid aortic valve, Breast Cancer, Breast Carcinoma, Breast neoplasm, Brugada syndrome, Carcinogenesis, Cardiac arrhythmias, Cardiovascular disease, Cerebral palsy, Colorectal Cancer, Congenital heart defect, Congenital Heart Disease, Congestive Heart Failure, Coronary Heart Disease, Diabetes Mellitus, Diabetic cardiomyopathy, Dilated Cardiomyopathy, Double outlet right ventricle, Hearing Loss, Heart Diseases, Heart Failure, Hypertension, Hypertrophic Subaortic Stenosis, Hypoplastic Left Heart Syndrome, Inclusion body myopathy, Ischemic stroke, Kabuki Syndrome, Lipoatrophy, Lipodystrophy, Liver carcinoma, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Melanoma, Microvascular angina, Myocardial Infarction, Myocarditis, Myopathy, Neoplasms, Obesity, Obstructive Asymmetric Septal Hypertrophy, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Patent foramen ovale, Persistent Ostium Primum, Prostate cancer, Rhabdomyosarcoma, Scoliosis, Secundum atrial septal defect, Septal Hypertrophy, Shone Complex, Sick Sinus Syndrome, Sinus Node Dysfunction, Sinus venosus atrial septal defect, Skin cancer, Squamous cell carcinoma, Stomach neoplasms, Stroke, Subaortic Stenosis, Tricuspid atresia, Wolff-Parkinson-White Syndrome
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4253
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|
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Myosin heavy chain 7 |
CMD1S, CMH1, CMYO7A, CMYO7B, CMYP7A, CMYP7B, MPD1, MYHCB, SPMD, SPMM |
Curated: 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 syndrome, MYH7-related skeletal myopathy, dilated cardiomyopathy 1S
Unreviewed: Acquired Kyphoscoliosis, Amyotrophy, Aortic Valve Sclerosis, Aortic valve stenosis, Atrial Fibrillation, Atrial Septal Defect, Autism, Blood protein disorder, Bohring syndrome, Brugada Syndrome, Bulbar palsy, Bundle Branch Block, Cardiac arrhythmias, Cardiomegaly, Cardiovascular Abnormalities, Cardiovascular Diseases, Central core myopathy, Centronuclear Myopathy, Centronuclear Myopathy, X-Linked, Chronic Obstructive Pulmonary Disease, Cleft palate, Clubfoot, Congenital abnormalities, Congenital heart defect, Congenital heart septal defect, Congenital kyphoscoliosis, Congenital muscular dystrophy, Congenital myopathy with fiber type disproportion, Congenital Structural Myopathy, Congestive Heart Failure, Contracture, Coronary Stenosis, Cryptorchidism, Developmental delay, Diabetes mellitus, Dilated Cardiomyopathy, Disorder Of Skeletal Muscle, Distal Muscular Dystrophy, Distal Myopathy, Double outlet right ventricle, Dwarfism, Dysphagia, Ebstein anomaly of the tricuspid valve, Emery-Dreifuss Muscular Dystrophy, X-Linked, Endocardial Fibroelastosis, Epilepsy, Fabry disease, Facial paralysis, Facioscapulohumeral Muscular Dystrophy, Genetic predisposition to disease, Head and neck neoplasm, Hearing Loss, Heart disease, Heart Diseases, Heart Failure, Heart Septal Defects, Hereditary Hemochromatosis, High palate, Hyaline Body Myopathy, Hydrocephalus, Hyperlipoproteinemia, Hypertrophic Subaortic Stenosis, Hypertrophy, Hypocalciuric Hypercalcemia, Hypoplastic Left Heart Syndrome, Hypotonia, Immunologic Deficiency Syndromes, Isolated systolic hypertension, Kidney failure, Lamellar ichthyosis, Left anterior fascicular block, Left Ventricular Hypertrophy, Left ventricular noncompaction, Leopard syndrome, Limb amyotrophy, Limb Muscle Atrophy, Lipoatrophy, Lipodystrophy, Long QT Syndrome, Lung neoplasms, Lymphatic metastasis, Lymphopenia, Lysinuric Protein Intolerance, Malocclusion, Melas syndrome, Mental retardation, Minicore myopathy with external ophthalmoplegia, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial encephalopathy, Mitochondrial myopathy, Mitral Valve Prolapse, Motor neuron disease, Multiminicore Myopathy, Myeloproliferative disorder, Myocardial Diseases, Myocardial Infarction, Myofibrillar myopathy, Myotonia congenita, Nephrotic syndrome, Neuromuscular Diseases, Noncompaction cardiomyopathy, Obesity, Obstructive Asymmetric Septal Hypertrophy, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Paroxysmal ventricular fibrillation, Patent ductus arteriosus, Prostatic neoplasm, Ptosis, Right ventricular hypertrophy, Scapuloperoneal Muscular Dystrophy, Scoliosis, Seizures, Septal Hypertrophy, Severe combined immunodeficiency disease, Sleep Apnea, Spinal Muscular Atrophy, Squamous cell carcinoma, Stroke, Subaortic Stenosis, Tibial muscular dystrophy, Toe extensor amyotrophy, Tubular Aggregate Myopathy, Vascular calcification, Ventricular arrhythmia, Ventricular dysfunction, Ventricular Failure, Ventricular fibrillation, Ventricular hypertrophy, Ventricular remodeling, Ventricular septal defect, Ventricular tachycardia, Welander Distal Myopathy, Wolff-Parkinson-White Syndrome
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4254
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|
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Myosin heavy chain 7B |
MHC14, MYH14, lncMYH7b |
Curated: Brugada syndrome, Dilated cardiomyopathy, Cardiomyopathy, Thromboembolic pulmonary hypertension, Congenital left-sided heart lesions, Hypertrophic cardiomyopathy, Left ventricular disease, Melanoma, Non-melanoma skin carcinoma
Unreviewed: Bipolar disorder, Cardiomegaly, Colorectal Cancer, Colorectal neoplasm, Congenital myopathy, Congenital myopathy with fiber type disproportion, Hearing loss, Hypoplastic Left Heart Syndrome, Left ventricular noncompaction, Myotonia congenita
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4255
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|
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Myosin heavy chain 8 |
DA7, MyHC-peri, MyHC-pn, gtMHC-F |
Curated: Arthrogryposis multiplex congenita, Distal arthrogryposis, Carney complex, Hecht syndrome, Neuromuscular disease, Trismus-pseudocamptodactyly syndrome, Venous thromboembolism
Unreviewed: Atrial myxoma, Breast neoplasm, Bulbospinal Atrophy, X-Linked, Carcinogenesis, Carney Complex, Carney complex variant, Clubfoot, Congenital Clubfoot, Congenital contracture, Congenital Retrognathism, Contracture, Cushing syndrome, Dwarfism, Dysphagia, Endometriosis, Leukemia, Malignant Neoplasm, Malocclusion, Micrognathism, Monocytic Leukemia, Myopathy, Myxoma, Myxoma Of Heart, Myxoma Of The Endocardium, Neoplasms, Ovarian diseases, Parkinson disease, Ptosis, Sarcopenia, Syndactyly Of The Toes, Trismus, Trismus-Pseudocamptodactyly Syndrome
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4256
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|
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Myosin heavy chain 9 |
BDPLT6, DFNA17, EPSTS, FTNS, MATINS, MHA, NMHC-II-A, NMMHC-IIA, NMMHCA |
Curated: 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 loss, Hereditary hearing loss, Renal hypertension, Hypertension, Hypertensive nephropathy, Kidney failure, Meniere disease, Nephrotic syndrome, Obesity, Orofacial cleft, Sebastian syndrome, Thrombocytopenia, Uterine fibroid, macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss
Unreviewed: Adenocarcinoma, Alloimmune Thrombocytopenia, Alport Syndrome, Alport Syndrome, X-Linked, Amyotrophic Lateral Sclerosis, Anaplastic Lymphoma, Andersen Syndrome, Anemia, Anodontia, Anxiety Disorder, Appendicitis, Arterial Tortuosity Syndrome, Arteriosclerosis, Asthenozoospermia, Atherosclerosis, Autoimmune Diseases, Bernard Soulier Syndrome, Bernard-soulier syndrome, Bipolar disorder, Bladder exstrophy, Blood coagulation disorder, Blood Coagulation Disorders, Breast Cancer, Breast Carcinoma, Breast neoplasm, Capillary malformation, Carcinogenesis, Carcinoma, Carotid Artery Thrombosis, Cataract, Cerebrovascular Disorders, Cleft Lip With Or Without Cleft Palate, Colorectal Cancer, Colorectal neoplasm, Congenital Cataract, Congenital thrombocytopenia, Craniosynostosis, Deafness, Nonsyndromic Sensorineural, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Ear Diseases, Ectodermal dysplasia, Eosinophilia, Epstein syndrome, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Fechtner syndrome, Focal segmental glomerulosclerosis, Fraser syndrome, Giant Platelet Syndrome With Thrombocytopenia, Glioma, Glomerular Hyalinosis, Glomerulosclerosis, Graft-versus-host disease, Graft-Vs-Host Disease, Gray Platelet Syndrome, Head and neck cancer, Head And Neck Carcinoma, Head and neck neoplasm, Headache, Hearing Loss, Heart failure, Hemangioma, Hematologic disease, Hematuria, Hemorrhage, Hemorrhagic disease, Hemorrhoids, Hepatocellular carcinoma, Hereditary Nephritis, Hereditary neuropathy with liability to pressure palsies, Immune Thrombocytopenic Purpura, Kidney Disease, Kidney Failure, Leukemia, Lung Cancer, Lung carcinoma, Lupus Nephritis, Lymphatic metastasis, Macrothrombocytopenia, MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS, Malformation of cortical development, Malignant Neoplasm, Mammary Neoplasms, Marfan Syndrome, Membranous Glomerulonephritis, Mesothelioma, Monocytic Leukemia, Multiple sclerosis, Myeloid leukemia, Myelomonocytic Leukemia, MYH9-Related Disease, Myocardial Infarction, Myotonic dystrophy, Nasopharyngeal Carcinoma, Neoplasms, Nephritis, Nephrosclerosis, Nephrotic Syndrome, Neuroblastoma, Neutropenia, Nodular Fasciitis, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Orofacial Cleft, Otitis media, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic ductal carcinoma, Pancytopenia, Papillary thyroid cancer, Papillary thyroid carcinoma, Platelet disorder, Platelet-type bleeding disorder, Portal Vein Thrombosis, Presenile Cataract, Prostatic neoplasm, Proteinuria, Renal Carcinoma, Renal Glomerular Disease, Renal Hypertension, Renal Insufficiency, Sarcoma, Schizophrenia, SEBASTIAN SYNDROME, Seizures, Sickle cell anemia, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Thrombosis, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Trichohepatoenteric Syndrome, Triple negative breast cancer, Uterine neoplasm
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4257
|
|
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MYH9 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
4258
|
|
|
Myosin heavy chain gene cluster antisense RNA |
linc-MYH |
Curated: N/A
Unreviewed: Carney Complex, Hecht syndrome, Inclusion body myopathy, Laryngeal neoplasm, Myopathy
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4259
|
|
|
Myosin light chain 1 |
CMYO14, CMYP14, MLC-1, MLC1, MLC1/3, MLC1F, MLC3F, MYOFTA |
Curated: Congenital myopathy, Cardiac injury
Unreviewed: Aortic valve disease, Breast neoplasm, Congenital Myopathy With Reduce Muscle Fibers, Developmental disability, Dilated cardiomyopathy, High palate, Hypertrophic cardiomyopathy, Left ventricular disease, Motor delay, Myosin storage myopathy, Myotonia congenita, Neoplasms, Rhabdomyosarcoma, Squamous cell carcinoma
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4260
|
|
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Myosin light chain 10 |
MYLC2PL, PLRLC |
Curated: 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
Unreviewed: N/A
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