|
701
|
|
|
Titin |
CMD1G, CMH9, CMPD4, CMYO5, CMYP5, EOMFC, HMERF, LGMD2J, LGMDR10, MYLK5, SALMY, TMD |
Acne, Amyotrophy, Arrhythmogenic right ventricular cardiomyopathy, Arthrogryposis multiplex congenita, Atrial fibrillation, Atrial septal defect, Atrioventricular block, Av nodal reentry tachycardia, Biventricular hypertrophy, Bladder carcinoma, Cardiomyopathy, Centronuclear myopathy, Charcot-marie-tooth disease, Colorectal cancer, Complete atrioventricular block, Congenital clubfoot, Congenital muscular dystrophy, Congenital myopathy, Congenital torticollis, Congestive heart failure, Developmental delay, Dilated cardiomyopathy, Distal muscular dystrophy, Distal myopathy, Dwarfism, Dysarthria, Facial paralysis, Gastric cancer, Hearing loss, Heart failure, Hereditary myopathy with early respiratory failure, High palate, Hip contracture, Hypertrophic cardiomyopathy, Infiltrating duct carcinoma of female breast, Left ventricular hypertrophy, Left ventricular noncompaction, Leukemia, Limb-girdle muscular dystrophy, Lipoatrophy, Lipodystrophy, Lung carcinoma, Lung adenocarcinoma, Malocclusion, Mental retardation, Metastatic melanoma, Microstomia, Mitral valve prolapse, Motor delay, Multiminicore myopathy, Multiple congenital anomalies, Muscular dystrophy, Myofibrillar myopathy, Myopathy, Myopathy with fatal cardiomyopathy, Myopia, Neck webbing, Necrotizing myopathy, Nephroblastoma, Neuromuscular diseases, Noncompaction cardiomyopathy, Ovarian adenocarcinoma, Ovarian serous adenocarcinoma, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Peroneal muscle atrophy, Progressive contractures-limb-girdle weakness-muscle dystrophy syndrome, Ptosis, Pulmonary arterial hypertension, Pulmonary stenosis, Respiratory failure, Scoliosis, Thoracolumbar scoliosis, Tibial muscular dystrophy, Ventricular arrhythmia, Ventricular failure, Ventricular hypertrophy, Ventricular tachycardia, Welander distal myopathy, Wolff-parkinson-white syndromeView all (65 more) |
|
702
|
|
|
Alpha tocopherol transfer protein |
ATTP, AVED, TTP1, alphaTTP |
Ataxia, Atherosclerosis, Clinodactyly, Developmental delay, Developmental regression, Diabetes mellitus, Dysarthria, Dyslalia, Eyelid xanthoma, Friedreich ataxia, Hemeralopia, Hemiplegia/hemiparesis, Hypercholesterolemia, Hypertrophic cardiomyopathy, Mental retardation, Microstomia, Nervous system disorder, Nyctalopia, Nystagmus, Posteriorly rotated ear, Retinal diseases, Retinitis pigmentosa, Scoliosis, Sensory neuropathy, Somatosensory disorders, Speech disorders, Urination disorders, Vision disability, Vitamin e deficiency, Xanthoma, Xanthoma tendinosumView all (16 more) |
|
703
|
|
|
TUB bipartite transcription factor |
RDOB, rd5 |
Astigmatism, Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Mental retardation, Myopia, Nystagmus, Obesity, Optic atrophy, Optic neuropathy, Retinal dystrophy, Retinal dystrophy and obesity, Retinitis pigmentosa, Rod-cone dystrophyView all (4 more) |
|
704
|
|
|
Transthyretin |
ATTR, CTS, CTS1, HEL111, HsT2651, PALB, TBPA, TTN |
Amyloid cardiomyopathy, Amyloid neuropathy, Amyloid polyneuropathy, Amyloidogenic transthyretin amyloidosis, Amyloidosis, Amyloidosis, leptomeningeal, transthyretin-related, Anemia, Atrioventricular block, Attrv122i amyloidosis, Cardiomyopathy, Carpal tunnel syndrome, Dementia, Dysarthria, Dysautonomia, Dystransthyretinemic euthyroidal hyperthyroxinemia, Erectile dysfunction, Multiple polyposis syndrome, Kidney disease, Kidney failure, Lung neoplasms, Lung cancer, Mental depression, Myofibrillar myopathy, Nervous system diseases, Nystagmus, Pancytopenia, Paraplegia, Peripheral axonal neuropathy, Polyneuropathy, Acute kidney insufficiency, Senile cardiac amyloidosis, Sensorimotor neuropathy, Transthyretin-related amyloid cardiomyopathy, Trigger finger disorderView all (19 more) |
|
705
|
|
|
Tubulin alpha 4a |
ALS22, CMYO26, FTDALS9, H2-ALPHA, OZEMA23, SPAX11, TUBA1 |
|
|
706
|
|
|
Tubulin beta 2A class IIa |
CDCBM5, TUBB, TUBB2 |
Arthritis, Colorectal cancer, Cortical dysplasia, Cortical dysplasia with other brain malformations, Creutzfeldt-jakob disease, Developmental delay, Hypoplasia of corpus callosum, Juvenile arthritis, Leukemia, Myeloid leukemia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease |
|
707
|
|
|
Tubulin gamma 1 |
CDCBM4, GCP-1, TUBG, TUBGCP1 |
|
|
708
|
|
|
Tu translation elongation factor, mitochondrial |
COXPD4, EF-TuMT, EFTU, P43 |
|
|
709
|
|
|
Tuftelin 1 |
WHSF |
|
|
710
|
|
|
TUB like protein 1 |
LCA15, RP14, TUBL1 |
Anetoderma, Brachydactyly, Capsular cataract, Cataract, Ciliopathies, Congenital cerebral hernia, Congenital hypoplasia of penis, Congenital nystagmus, Developmental delay, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hemiplegia/hemiparesis, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Myopia, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Polydactyly, Retinal diseases, Retinitis pigmentosa, Rod-cone dystrophy, SyndactylyView all (15 more) |
