|
241
|
|
|
Translocase of inner mitochondrial membrane 10 |
TIM10, TIM10A, TIMM10A |
|
|
242
|
|
|
Tetraspanin 16 |
TM-8, TM4-B, TM4SF16 |
|
|
243
|
|
|
Transducin beta like 2 |
WBSCR13, WS-betaTRP |
Abnormal dermatoglyphic pattern, Abnormal spinal segmentation, Accessory kidney, Aneurysm of aortic arch, Anxiety disorder, Arnold-chiari malformation, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bicuspid aortic valve, Bladder diverticulum, Blepharophimosis, Camptodactyly of fingers, Cataract, Cerebral cortical atrophy, Cholelithiasis, Congenital anomaly of neck, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital pectus excavatum, Congestive heart failure, Cornea plana, Cryptorchidism, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dysgraphia, Esophagus neoplasm, Gastroesophageal reflux disease, Glaucoma, Gout, Gouty arthritis, Hearing loss, Hypercalcemia, Hypertension, Hypertrophic cardiomyopathy, Hypodontia, Hypogonadotropic hypogonadism, Hypothyroidism, Macroglossia, Macrostomia, Macrotia, Malabsorption syndrome, Mental depression, Mental retardation, Microcephaly, Microdontia, Micrognathism, Mitral valve prolapse, Multiple renal cysts, Myocardial infarction, Myopathy, Myopia, Nephrocalcinosis, Nephrolithiasis, Nystagmus-induced head nodding, Obesity, Obsessive-compulsive disorder, Osteopenia, Osteoporosis, Osteosclerosis, Otitis media, Overriding aorta, Patent ductus arteriosus, Pelvic kidney, Peptic ulcer, Peripheral pulmonary artery stenosis, Phakomatosis pigmentovascularis, Polycystic ovary syndrome, Posterior embryotoxon, Precocious puberty, Pulmonary stenosis, Radioulnar synostosis, Rectal prolapse, Renal hypoplasia, Renal insufficiency, Scoliosis, Spina bifida occulta, Strabismus, Stroke, Supravalvar aortic stenosis, Tetralogy of fallot, Ventricular septal defect, Vesicoureteral reflux, Williams syndromeView all (73 more) |
|
244
|
|
|
Thiamin pyrophosphokinase 1 |
HTPK1, PP20, THMD5 |
|
|
245
|
|
|
TRNA methyltransferase 2A |
HTF9C |
|
|
246
|
|
|
Trafficking protein particle complex subunit 3 |
BET3 |
|
|
247
|
|
|
Tight junction protein 3 |
ZO-3, ZO3 |
|
|
248
|
|
|
Tubulin gamma complex component 4 |
76P, GCP-4, GCP4, Grip76, MCCRP3 |
Cerebral cortical atrophy, Chorioretinopathy-microcephaly syndrome, Developmental delay, Dwarfism, Malformation of cortical development, Mental retardation, Microcephaly, Microcephaly with chorioretinopathy, Microphthalmos, Nystagmus, Optic atrophy, Scoliosis, Strabismus |
|
249
|
|
|
TNF receptor superfamily member 21 |
BM-018, CD358, DR6 |
|
|
250
|
|
|
Tubulointerstitial nephritis antigen |
TIN-AG |
|
