|
441
|
|
|
THO complex subunit 2 |
AMC7, CXorf3, MRX12, MRX35, THO2, XLID12, dJ506G2.1, hTREX120 |
Anxiety disorder, Autism, Dwarfism, Dysmorphic features, High palate, Mental retardation, Intellectual disability-short stature-overweight syndrome, x-linked, Isolated somatotropin deficiency, Macrotia, Mental depression, Mental retardation, x-linked, Microcephaly, Myocardial infarction, Nystagmus, Penis agenesis, Pulmonary fibrosis, Seizure, Somatotropin deficiency, Stereotyped behavior, StrabismusView all (5 more) |
|
442
|
|
|
THAP domain containing 11 |
CTG-B43a, CTG-B45d, HRIHFB2206, MAHCL, RONIN, SCA51 |
|
|
443
|
|
|
Tetratricopeptide repeat domain 7A |
GIDID, MINAT, TTC7 |
Absent eyebrow, Autoimmune hemolytic anemia, Congenital atresia of colon, Congenital atresia of ileum, Congenital atresia of pulmonary valve, Congenital cystic adenomatoid malformation of lung, Congenital hypoplasia of thymus, Congenital malrotation of intestine, Congenital omphalocele, Congenital pyloric atresia, Diabetes mellitus, Erectile dysfunction, Gastrointestinal atresia, Hashimoto disease, Intestinal atresia, Jejunal atresia, Multiple gastrointestinal atresias, Nail dystrophy, Prostate cancer, Psoriasiform eczema, Severe combined immunodeficiency disease, Ventricular septal defectView all (7 more) |
|
444
|
|
|
Tweety family member 1 |
- |
|
|
445
|
|
|
Teneurin transmembrane protein 2 |
ODZ2, TEN-M2, TEN2, TNM2, ten-2 |
|
|
446
|
|
|
TBC1 domain family member 24 |
DEE16, DFNA65, DFNB86, DOORS, EIEE16, EIM, EPRPDC, FIME, TLDC6 |
Action myoclonus-renal failure syndrome, Adrenal hyperplasia, Ambiguous genitalia, Anonychia, Arrhinencephaly, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Cerebral atrophy, Congenital adrenal hyperplasia, Congenital clubfoot, Congenital epicanthus, Congenital hypothyroidism, Congenital nystagmus, Dandy-walker syndrome, Deafness, Dentatorubral pallidoluysian atrophy, Developmental delay, Developmental regression, Digitorenocerebral syndrome, Doors syndrome, Double outlet right ventricle, Dysarthria, Dyscognitive seizures, Epilepsy, Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer`s cramp, Epileptic encephalopathy, Febrile seizures, Focal epilepsy-intellectual disability-cerebro-cerebellar malformation, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Hemifacial seizures, Hereditary leber optic atrophy, High palate, Horizontal nystagmus, Hydronephrosis, Inclusion-body disease, Language disorders, Lumbar scoliosis, Malignant migrating partial seizures of infancy, May-white syndrome, Mental retardation, Microcephaly, Movement disorders, Myoclonic epilepsy, Myoclonic seizures, Myopia, Nail diseases, Nail dysplasia, Nail dystrophy, Nephrocalcinosis, Nervous system diseases, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Optic atrophy, Parkinson disease, Periodic paralysis, Photosensitive tonic-clonic seizures, Polymicrogyria, Polyneuropathy, Progressive myoclonic epilepsy with dystonia, Proteasome-associated autoinflammatory syndrome, Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer`s cramp syndrome, Sagittal craniosynostosis, Seizure, Sensorineural hearing loss, Sirenomelia, Spina bifida occulta, Status epilepticus, Strabismus, Strawberry nevus of skin, Thrombocytosis, Writer`s crampView all (62 more) |
|
447
|
|
|
TAO kinase 1 |
DDIB, KFC-B, MAP3K16, MARKK, PSK-2, PSK2, TAO1, hKFC-B, hTAOK1 |
|
|
448
|
|
|
Twinfilin actin binding protein 1 |
A6, PTK9 |
|
|
449
|
|
|
TRNA methyltransferase 5 |
COXPD26, KIAA1393, PNSED, TRM5 |
|
|
450
|
|
|
Transmembrane protein 181 |
GPR178, KIAA1423 |
|
