|
731
|
|
|
Trafficking protein particle complex subunit 6A |
TRS33 |
|
|
732
|
|
|
TATA-box binding protein associated factor, RNA polymerase I subunit D |
JOSD3, RAFI41, TAF(I)41, TAFI41 |
|
|
733
|
|
|
Transmembrane protein 43 |
ARVC5, ARVD5, AUNA3, EDMD7, EDMD7; AUNA2, LUMA |
Amyotrophy, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Atrioventricular block, Cardiomyopathy, Congenital pectus excavatum, Congestive heart failure, Dyskinetic syndrome, Elbow flexion contracture, Emery-dreifuss muscular dystrophy, Emery-dreifuss muscular dystrophy, x-linked, Hypertrophic cardiomyopathy, Ichthyosis, Limb-girdle muscular dystrophy, Lipodystrophy, Muscular dystrophy, Obesity, Ptosis, Scoliosis, Sprengel deformity, Ventricular cardiomyopathy, Ventricular tachycardia, Vocal cord paralysisView all (8 more) |
|
734
|
|
|
THO complex subunit 6 |
MMRFCGU, WDR58, fSAP35 |
Blepharophimosis, Congenital epicanthus, Cryptorchidism, Developmental delay, Developmental delay-microcephaly-facial dysmorphism syndrome, Dysmorphic features, Endometriosis, Horseshoe kidney, Mental retardation, Microcephaly, Multiple congenital anomalies, Myopia, Patent ductus arteriosus, Plagiocephaly, Renal agenesis, Sprengel deformity, Synophrys, Ventricular septal defectView all (3 more) |
|
735
|
|
|
Transcription factor EB |
ALPHATFEB, BHLHE35, TCFEB |
|
|
736
|
|
|
Transmembrane protein 231 |
ALYE870, JBTS20, MKS11, PRO1886 |
Anencephaly, Arima syndrome, Autism, Cataract, Cerebellar vermis agenesis, Ciliopathies, Asplenia, Congenital cerebral hernia, Congenital coloboma of iris, Congenital hepatic fibrosis, Congenital pectus excavatum, Coronary heart disease, Coronary syndrome, Cryptorchidism, Cystic liver disease, Dandy-walker syndrome, Developmental delay, Diastrophic dysplasia, Double ureter, Dysmorphic features, Exotropia, Eyelid myoclonias, Fibrosis of pancreas, Foot polydactyly, Fundus coloboma, Gastrointestinal stromal tumor, Hirschsprung disease, Hydrocephalus, Mental retardation, Joubert syndrome, Joubert syndrome with oculorenal defect, Keratosis follicularis, Kidney disease, Lobar holoprosencephaly, Male pseudohermaphroditism, Malformation of cortical development, Meckel syndrome, Meckel-gruber syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Mohr-tranebjaerg syndrome, Multicystic renal dysplasia, Nystagmus, Occipital encephalocele, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Orofaciodigital syndrome, Pancreatic cyst, Polycystic kidney disease, Polycystic liver disease, Polydactyly, Polydactyly of toes, Ptosis, Renal cyst, Renal insufficiency, Retinal coloboma, Retinal dystrophy, Sclerocornea, Scoliosis, Situs inversus, Strabismus, Syndromic microphthalmia, Talipes, True hermaphroditism, Postaxial hand polydactyly, Urethral atresiaView all (54 more) |
|
737
|
|
|
Tectonic family member 1 |
JBTS13, TECT1 |
Cerebellar vermis agenesis, Ciliopathies, Congenital cerebral hernia, Congenital coloboma of iris, Developmental delay, Disorder of eye, Hirschsprung disease, Hydrocephalus, Joubert syndrome, Mental retardation, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral cleft, Pachygyria, Polydactyly of toes, Polymicrogyria, Ptosis, Scoliosis, Situs inversus, StrabismusView all (6 more) |
|
738
|
|
|
Transport and golgi organization 6 homolog |
TMCO7 |
|
|
739
|
|
|
Terminal uridylyl transferase 7 |
PAPD6, TENT3B, ZCCHC6 |
|
|
740
|
|
|
TBL1X/Y related 1 |
C21, DC42, IRA1, MRD41, TBLR1 |
Anemia, Anorexia, Arnold-chiari malformation, Asthma, Autism, Benign neoplasm of bladder, Urinary bladder cancer, Bladder neoplasm, Bladder carcinoma, Brachycephaly, Central nervous system lymphoma, Colorectal cancer, Dislocated radial head, Cryptorchidism, Developmental delay, Diffuse alveolar hemorrhage, Disseminated intravascular coagulation, Dwarfism, Dysmorphic features, Fibrinogen deficiency, Gangrene, Hypofibrinogenemia, Leukopenia, Non-hodgkin lymphoma, Macrocephaly, Malignant mesothelioma, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Narcolepsy, Neurodevelopmental disorders, Neutropenia, Pancytopenia, Pendular nystagmus, Pierpont syndrome, Posteriorly rotated ear, Promyelocytic leukemia, Prostatic neoplasms, Prostate cancer, Respiratory tract diseases, Scoliosis, Spade-like hand, Stomatitis, Talipes transversoplanusView all (30 more) |
