|
231
|
|
|
Transmembrane protein 98 |
TADA1 |
|
|
232
|
|
|
TBC1 domain family member 29, pseudogene |
TBC1D29 |
|
|
233
|
|
|
Torsin 1A interacting protein 1 |
LAP1, LAP1B, LAP1C, LGMD2Y |
|
|
234
|
|
|
Tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 |
IDDALDS, ROLSA, rols |
|
|
235
|
|
|
Tectonic family member 3 |
C10orf61, JBTS18, OFD4, TECT3 |
Acquired kyphoscoliosis, Acquired porencephaly, Addison`s disease, Brachydactyly, Cerebellar vermis agenesis, Cerebral atrophy, Cerebral cortical hemiatrophy, Choanal atresia, Clinodactyly, Congenital atresia of rectum, Congenital camptodactyly, Congenital epicanthus, Congenital heart defects, Pulmonary hypoplasia, Congenital kyphoscoliosis, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Disorder of eye, Dwarfism, Esotropia, Frontal bossing, Hamartoma, Hearing loss, High palate, Horseshoe kidney, Hypothalamic hamartomas, Imperforate anus, Joubert syndrome, Laryngomalacia, Malformation of cortical development, Mental retardation, Microcephaly, Micrognathism, Micromelia, Monorchism, Nystagmus, Orofaciodigital syndrome, Polydactyly, Polydactyly of toes, Porencephalic cyst, Posteriorly rotated ear, Proptosis, Radial polydactyly, Renal agenesis, Specific learning disorder, Subcortical cerebral atrophy, Submucosal cleft palate, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Postaxial hand polydactyly, Ventricular septal defectView all (38 more) |
|
236
|
|
|
Transient receptor potential cation channel subfamily C member 4 associated protein |
C20orf188, PPP1R158, TRRP4AP, TRUSS |
|
|
237
|
|
|
Testin LIM domain protein |
TESS, TESS-2 |
|
|
238
|
|
|
Tubulin tyrosine ligase like 3 |
HOTTL |
|
|
239
|
|
|
TRAF3 interacting protein 1 |
CFAP116, FAP116, IFT54, MIP-T3, MIPT3, SLSN9 |
Astigmatism, Cataract, Congenital hepatic fibrosis, Developmental delay, Dwarfism, Hypertension, Jeune thoracic dystrophy, Kidney disease, Age-related macular degeneration, Majewski syndrome, Nephritis, Nephronophthisis, Nystagmus, Polydactyly, Premature menopause, Renal dysplasia and retinal aplasia, Retinal dystrophy, Rod-cone dystrophy, Senior-loken syndrome, Short rib-polydactyly syndrome, StrabismusView all (6 more) |
|
240
|
|
|
TERF1 interacting nuclear factor 2 |
DKCA3, DKCA5, TIN2 |
Alopecia, Anemia, Aplastic anemia, Bone marrow diseases, Cataract, Cerebellar diseases, Cerebellar hypoplasia, Cerebral cortical atrophy, Cirrhosis, Congenital keratoglobus, Cryptorchidism, Developmental delay, Diabetes mellitus, Dwarfism, Dyskeratosis congenita, Dyskeratosis congenita, x-linked, Esophageal stenosis, Excessive tearing, Exudative retinopathy, Hoyeraal-hreidarsson syndrome, Hypodontia, Hypoplasia of the maxilla, Immunologic deficiency syndromes, Leukocoria, Leukopenia, Leukoplakia, Liver failure, Lymphoma, Lymphopenia, Malabsorption syndrome, Mental retardation, Microcephaly, Myelodysplasia, Myelodysplastic syndrome, Nail diseases, Nail dysplasia, Nail dystrophy, Neoplasms, Nystagmus, Osteoporosis, Palmoplantar keratoderma, Pancreatic neoplasm, Periodontitis, Pulmonary fibrosis, Retinal diseases, Revesz syndrome, Scoliosis, Skin carcinoma, Specific learning disorder, TaurodontismView all (35 more) |
