4241
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MYG1 pseudogene 1 |
C12orf10P1 |
Curated: N/A
Unreviewed: N/A
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4242
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Myosin heavy chain 1 |
HEL71, MYHSA1, MYHa, MyHC-2X/D, MyHC-2x |
Curated: N/A
Unreviewed: Autoimmune Diseases, Breast Cancer, Breast neoplasm, Cerebral palsy, Chronic obstructive pulmonary disease, Epilepsy, Facioscapulohumeral muscular dystrophy, Focal segmental glomerulosclerosis, Glomerulosclerosis, Melanoma, MOHR-TRANEBJAERG SYNDROME, Myositis, Squamous cell carcinoma, Torre-Muir Syndrome, Vitamin D Deficiency
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4243
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Myosin heavy chain 10 |
NMMHC-IIB, NMMHCB |
Curated: Autism, Coloboma, Neurodevelopmental disorder, Congenital fibrosis of extraocular muscles, Congenital ocular coloboma, Congenital ptosis, Focal glomerulosclerosis, Major depressive disorder, Diabetes mellitus type 2, Visual disorder, complex neurodevelopmental disorder with or without congenital anomalies
Unreviewed: Aortic Aneurysm, Aqueductal Stenosis, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Autism Spectrum Disorder, Bipolar disorder, Breast Cancer, Breast Carcinoma, Carcinogenesis, Cardiac Defects, Developmental dysplasia of the hip, Glioma, Glomerular Hyalinosis, Glomerulosclerosis, Heart disease, Hydronephrosis, Immune System Diseases, Inflammatory Bowel Disease, Jacobsen Syndrome, Leukemia, Lung carcinoma, Lung Diseases, Melanoma, Myeloid leukemia, Myelomonocytic Leukemia, Neoplasms, Ovarian neoplasm, Paris-Trousseau Thrombocytopenia, Platelet-type bleeding disorder, Pulmonary Emphysema, Squamous cell carcinoma
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4244
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Myosin heavy chain 11 |
AAT4, FAA4, SMHC, SMMHC, SMMS-1, VSCM2 |
Curated: Aortic aneurysm, Atrial fibrillation, Bicuspid aortic valve, Intestinal pseudo-obstruction, Congenital aneurysm of ascending aorta, Congenital heart disease, Connective tissue disease, Coronary artery disease, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Heart failure, Hemorrhoid, Left ventricular disease, Myeloid leukemia, Lissencephaly, Loeys-dietz syndrome, Marfan syndrome, Megacystis microcolon intestinal hypoperistalsis syndrome, Myopia, Patent ductus arteriosus, Psoriasis, Schizophrenia, Tetralogy of fallot, Tricuspid valve disease, Uterine fibroid, Visceral myopathy, Wolff-parkinson-white syndrome, familial thoracic aortic aneurysm and aortic dissection
Unreviewed: Acute Myeloid Leukemia, Adenoma, Alzheimer disease, Aneurysm, Aortic Aneurysm, Aortic Diseases, Aortic dissection, Aortic Valve Insufficiency, Arachnodactyly, Arteriosclerosis, Asthma, Atherosclerosis, Berdon syndrome, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiac Neoplasms, Cardiovascular disease, Cerebral Artery Aneurysm, Chagas disease, Colonic neoplasm, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital abnormalities, Congenital Aneurysm Of Ascending Aorta, Congenital Chromosomal Disease, Congenital Exomphalos, Congenital heart defect, Congenital malrotation of intestine, Congenital omphalocele, Coronary Arteriosclerosis, Crisponi syndrome, Cryptorchidism, Cutis marmorata, Cystic medial necrosis, Cystic Medial Necrosis Of Aorta, Dementia, Descending aortic dissection, Diabetic neuropathy, Dilated cardiomyopathy, Dissecting Aortic Aneurysm, Dyspnea, Paroxysmal, Dystonia, Endometrial neoplasm, Endometriosis, Eosinophilia, Gallbladder neoplasm, Gastroparesis, GATA2 Deficiency, Gestational diabetes, Graves ophthalmopathy, Heart disease, Hyperplasia, Hypertension, Hypospadias, Intestinal Pseudoobstruction, Intracranial Aneurysm, Intraductal noninfiltrating carcinoma, Ischemic Stroke, Leiomyosarcoma, Leukemia, Leukopenia, Lung carcinoma, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Mastocytosis, Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome, Megakaryocytic Leukemia, Microcolon, Monocytic Leukemia, Multicystic renal dysplasia, Myeloblastic Leukemia, Myelodysplastic Syndrome, Myeloid Leukemia, Myeloid Leukemia With Abnormal Bone Marrow Eosinophils Inv(16)(P13q22) Or T(16;16)(P13;Q22), Myelomonocytic Leukemia, Necrosis, Neoplasms, Nephroblastoma, Neurofibromatosis, Ovarian neoplasm, Penile Hypospadias, Peripheral arterial stenosis, Peutz-Jeghers Syndrome, Polyposis Syndrome, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Pseudoxanthoma elasticum, Scoliosis, Smith-McCort Dysplasia, Stomach Neoplasms, Stroke, Subarachnoid hemorrhage, Sveinsson chorioretinal atrophy, Thoracic aortic aneurysm, Thoracic Aortic Aneurysm And Aortic Dissection, Thoracic disease, Thrombocytopenia, Transient Ischemic Attack, Trichohepatoenteric Syndrome, Tricuspid Valve Insufficiency, Urethral obstruction, Urinary bladder diseases, Urinary bladder neoplasms, Uterine neoplasm, Visceral Myopathy
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4245
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Myosin heavy chain 13 |
MyHC-IIL, MyHC-eo |
Curated: Coronary artery disease, Major depressive disorder, Neuroblastoma, Open angle glaucoma, Osteoarthritis, Periodontitis
Unreviewed: Alzheimer disease, Arthritis, Osteoarthrosis Deformans
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4246
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Myosin heavy chain 14 |
DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C, NMHC-II-C, PNMHH, myosin |
Curated: Isolated sensorineural deafness, Nonsyndromic hearing loss, Dilated cardiomyopathy, Charcot-marie-tooth disease, Deafness, Dental enamel hypoplasia, Hearing loss, Hereditary hearing loss, Meniere disease, Peripheral neuropathy myopathy hoarseness hearing loss syndrome, Peripheral neuropathy, Peripheral neuropathy, myopathy, hoarseness, and hearing, Prostatic neoplasms, nonsyndromic genetic hearing loss
Unreviewed: Amyotrophic lateral sclerosis, Arthritis, Bardet-Biedl Syndrome, Bone disease, Carcinogenesis, Cardiomegaly, Cardiomyopathy, Chronic obstructive pulmonary disease, Cleft Lip With Or Without Cleft Palate, Colorectal Cancer, Colorectal neoplasm, Congenital anomaly of limb, Congenital Clubfoot, Congenital heart septal defect, Congestive Heart Failure, Coronary artery disease, Crisponi syndrome, Critical illness, Cystinosis, Diabetes mellitus, type 2, Distal amyotrophy, Distal hereditary motor neuropathy, Duchenne muscular dystrophy, Facioscapulohumeral muscular dystrophy, Focal segmental glomerulosclerosis, Glycogen storage disease, Gout, Heart disease, Heart Failure, Hypertrophic cardiomyopathy, Kawasaki disease, Kidney Disease, Kidney failure, Leukemia, Low Anorectal Malformation, Lung adenocarcinoma, Lymphoma, Malignant Neoplasm, Melanoma, Motor nerve neuritis, Mouth disease, Myeloid leukemia, Myocarditis, Myopathy, Myosin storage myopathy, Myotonia congenita, Myotonic dystrophy, Neoplasms, Nervous System Diseases, Neuromuscular disease, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Osteoporosis, Pancreatic cancer, Pancreatic carcinoma, Pelvic organ prolapse, Peripheral Neuropathy, Peripheral Neuropathy, Myopathy, Hoarseness, And Hearing Loss, Polycystic kidney disease, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Rheumatic heart disease, Sensorineural hearing loss, Squamous cell carcinoma, Stroke, Tongue cancer, Vascular Diseases, Ventricular dysfunction
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4247
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Myosin heavy chain 15 |
- |
Curated: Anxiety disorder, Bipolar disorder, Hypothyroidism, Insomnia, Major depressive disorder, Metabolic syndrome, Microcephaly, Diabetes mellitus type 2
Unreviewed: Amyotrophic Lateral Sclerosis, Arteriosclerosis, Asthma, Atherosclerosis, Coronary artery disease, Nonsyndromic Deafness, Stroke
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4248
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Myosin heavy chain 16 |
MHC20, MYH16P, MYH5 |
Curated: Leukemia
Unreviewed: N/A
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4249
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Myosin heavy chain 2 |
CMYO6, CMYP6, IBM3, MYH2A, MYHSA2, MYHas8, MYPOP, MyHC-2A, MyHC-IIa |
Curated: Childhood-onset autosomal recessive myopathy with external ophthalmoplegia, Congenital myopathy, Muscular dystrophy, Myopathy, Myositis, myopathy, proximal, and ophthalmoplegia
Unreviewed: Amyotrophic lateral sclerosis, Anemia, Arthrogryposis multiplex congenita, Blood Coagulation Disorders, Breast Cancer, Breast Carcinoma, Carcinoma Of The Head And Neck, Cardiomyopathy, Cerebral palsy, Clubfoot, Colitis, Colorectal neoplasm, Congenital Clubfoot, Congenital contracture, Contracture, Cryptorchidism, Cystinosis, Deglutition disorder, Dermatomyositis, Diabetic Nephropathy, Distal myopathy, External Ophthalmoplegia, Fanconi Anemia, Friedreich Ataxia, Frontotemporal dementia, Glioblastoma, Glioma, Hearing Loss, Hepatocellular carcinoma, Hereditary continuous muscle fiber activity, Hereditary Inclusion Body Myopathy-Joint Contractures-Ophthalmoplegia Syndrome, High palate, Hodgkin disease, Hydrocephalus, Hyperlipoproteinemia, Inclusion body myopathy, Kidney Disease, Lymphocytic Leukemia, Macrothrombocytopenia, Malignant Neoplasm, Melanoma, Myopathy With External Ophthalmoplegia, Myosin storage myopathy, Myotonia congenita, Nasopharyngeal carcinoma, Nemaline myopathy, Neoplasms, Neural Tube Defect, Neurofibromatosis, Neuromuscular Diseases, Oculopharyngodistal myopathy, Ophthalmoplegia, Osteoarthritis, Osteogenesis imperfecta, Pleural effusion, Polyarthralgia, Polymyositis, Renal Glomerular Disease, SEBASTIAN SYNDROME, Squamous cell carcinoma, Synovitis, Tremor
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4250
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Myosin heavy chain 3 |
CPSFS1A, CPSFS1B, CPSKF1A, CPSKF1B, DA2A, DA2B, DA2B3, DA8, HEMHC, MYHC-EMB, MYHSE1, SMHCE |
Curated: 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
Unreviewed: Abnormal spinal segmentation, Acquired Kyphoscoliosis, Aortic Aneurysm, Basilar invagination, Blepharophimosis, Carpal synostosis, Cerebellar atrophy, Chronic obstructive pulmonary disease, Clubfoot, Colonic neoplasm, Congenital abnormalities, Congenital alveolar dysplasia, Congenital Camptodactyly, Congenital Clubfoot, Congenital contracture, Congenital Epicanthus, Congenital Exomphalos, Congenital heart septal defect, Congenital Hypoplasia Of Penis, Congenital kyphoscoliosis, Congenital Pectus Excavatum, Congenital Retrognathism, Contracture, Cryptorchidism, Digitotalar Dysmorphism, Dolichocephaly, Dwarfism, Dysmorphism, Elbow flexion contracture, Flexion Contracture Of Wrist, Freeman-Sheldon Syndrome, Head and neck neoplasm, Hearing Loss, High palate, Hip Contracture, Hypogonadism, Impaired Cognition, Klippel Feil syndrome, Malocclusion, Microcephaly, Micrognathism, Microstomia, Motor delay, Multiple Pterygium Syndrome, Myopathy, Neck Webbing, Neuromuscular disease, Nevus, Pterygium, Ptosis, Pulmonary hypoplasia, Rib fusion, Scoliosis, Scott Syndrome, Sheldon-Hall syndrome, Shoulder flexion contracture, Speech Disorders, Spina bifida occulta, Spondylocarpotarsal Synostosis Syndrome, Strabismus, Syndactyly of fingers, Talipes, Tarsal Coalition, Vertical Talus
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