|
861
|
|
|
Tetraspanin 18 |
TSPAN |
|
|
862
|
|
|
TATA-box binding protein associated factor, RNA polymerase I subunit A |
MGC:17061, RAFI48, SL1, TAFI48 |
|
|
863
|
|
|
THAP domain containing 3 |
- |
|
|
864
|
|
|
TOPBP1 interacting checkpoint and replication regulator |
C15orf42, SLD3, Treslin |
|
|
865
|
|
|
Transmembrane protein 263 |
C12orf23 |
|
|
866
|
|
|
Transducin beta like 1 Y-linked |
DFNY2, TBL1 |
|
|
867
|
|
|
TENM3 antisense RNA 1 |
TENM3-AS2 |
|
|
868
|
|
|
T-box transcription factor 19 |
TBS19, TPIT, dJ747L4.1 |
|
|
869
|
|
|
T-box transcription factor 18 |
CAKUT2, PUJO |
|
|
870
|
|
|
Transmembrane protein 67 |
JBTS6, MECKELIN, MKS3, NPHP11, TNEM67 |
Anemia, Anencephaly, Bardet-biedl syndrome, Brachydactyly, Cataract, Cerebellar vermis agenesis, Ciliopathies, Cirrhosis, Coloboma of optic disc, Asplenia, Congenital cerebral hernia, Congenital coloboma of iris, Congenital hepatic fibrosis, Congenital ocular coloboma, Cryptorchidism, Cystic kidney disease, Cystic liver disease, Dandy-walker syndrome, Developmental delay, Diastrophic dysplasia, Disorder of eye, Double ureter, Dwarfism, Dysmorphic features, Exotropia, Fibrosis of pancreas, Foot polydactyly, Fundus coloboma, Hearing loss, Hirschsprung disease, Hydrocephalus, Hypertension, Mental retardation, Isolated somatotropin deficiency, Joubert syndrome, Joubert syndrome with congenital hepatic fibrosis, Joubert syndrome with hepatic defect, Keratosis follicularis, Kidney disease, Liver neoplasms, Liver cirrhosis, Liver failure, Liver fibrosis, Lobar holoprosencephaly, Macrocephaly, Macrostomia, Male pseudohermaphroditism, Malformation of cortical development, Meckel syndrome, Meckel-gruber syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Mohr-tranebjaerg syndrome, Movement disorders, Multicystic renal dysplasia, Multiple congenital anomalies, Multiple small medullary renal cysts, Nephronophthisis, Nystagmus, Obesity, Occipital encephalocele, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Oral cleft, Osteochondrodysplasia, Osteopenia, Pancreatic cyst, Pancreatitis, Polycystic liver disease, Polydactyly, Polydactyly of toes, Polymicrogyria, Portal hypertension, Ptosis, Renal corticomedullary cysts, Renal insufficiency, Retinal coloboma, Rhyns syndrome, Rod-cone dystrophy, Sclerocornea, Scoliosis, Hypothyroidism, Senior-boichis syndrome, Situs inversus, Skeletal dysplasia, Somatotropin deficiency, Spastic paraplegia, Strabismus, Syndromic microphthalmia, Talipes, True hermaphroditism, Postaxial hand polydactyly, Urethral atresiaView all (81 more) |
