|
491
|
|
|
- |
- |
Cardiomyopathy, Deafness, nonsyndromic sensorineural, mitochondrial, Hearing loss, Melas syndrome, Merrf syndrome, Mitochondrial hypomagnesemia, hypertension, and hypercholesterolemia, Myoclonic seizures, Myopathy |
|
492
|
|
|
T-box transcription factor T |
SAVA, T, TFT |
Acrania, Anencephaly, Cervical spina bifida aperta, Cervical spina bifida cystica, Cervicothoracic spina bifida, Chordoma, Craniorachischisis, Diastematomyelia, Hydrocephalus, Imperforate anus, Lipoma, Lumbosacral spina bifida aperta, Lumbosacral spina bifida cystica, Meningomyelocele, Multiple lipomata, Neural tube defect, Neurenteric cyst, Primary tethered cord syndrome, Sacral agenesis, Sacral agenesis with vertebral anomalies, Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome, Spina bifida, Spina bifida cystica, Spina bifida occulta, Spinal cord myelodysplasia, Thoracolumbosacral spina bifida aperta, Thoracolumbosacral spina bifida cystica, Upper thoracic spina bifida aperta, Upper thoracic spina bifida cysticaView all (14 more) |
|
493
|
|
|
Tachykinin precursor 1 |
Hs.2563, NK2, NKNA, NPK, TAC2 |
Amnesia, Anorexia, Bipolar disorder, Bronchial hyperreactivity, Cirrhosis, Common migraine, Corneal diseases, Gastroesophageal reflux disease, Hyperemia, Involutional depression, Involutional paraphrenia, Manic disorder, Mental depression, Mood disorder, Narcolepsy, Narcolepsy-cataplexy syndrome, Psychosis, SchizophreniaView all (3 more) |
|
494
|
|
|
Tachykinin receptor 2 |
NK2R, NKNAR, SKR, TAC2R |
|
|
495
|
|
|
Tachykinin precursor 3 |
HH10, LncZBTB39, NK3, NKB, NKNB, PRO1155, ZNEUROK1 |
Anxiety disorder, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Erectile dysfunction, Female hypogonadism syndrome, Gynecomastia, Hypogonadism, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Mental depression, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Osteopenia, Osteoporosis, Penis agenesis, Physiologic amenorrhea, Secondary physiologic amenorrhea, Testicular hypogonadismView all (6 more) |
|
496
|
|
|
Transforming acidic coiled-coil containing protein 1 |
Ga55 |
|
|
497
|
|
|
Tachykinin receptor 1 |
NK1R, NKIR, SPR, TAC1R |
|
|
498
|
|
|
Tachykinin receptor 3 |
HH11, NK-3R, NK3, NK3R, NKR, TAC3R, TAC3RL |
Anxiety disorder, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Gynecomastia, Hearing loss, Hypogonadism, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mental depression, Mirror movements, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Schizophrenia, Secondary physiologic amenorrhea, Skeletal dysplasia, Testicular hypogonadismView all (20 more) |
|
499
|
|
|
TATA-box binding protein associated factor 1 |
BA2R, CCG1, CCGS, DYT3, DYT3/TAF1, KAT4, MRXS33, N-TAF1, NSCL2, OF, P250, TAF(II)250, TAF2A, TAFII-250, TAFII250, XDP |
Aplasia cutis congenita, Autism, Blepharospasm, Cerebellar atrophy, Colorectal cancer, Congenital epicanthus, Developmental delay, Dystonia, Dystonia-parkinsonism, x-linked, Expressive language delay, High palate, Hypoplasia of corpus callosum, Intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome, x-linked, Laryngospasm, Lipoma, Spastic diplegia, Macrotia, Mental retardation, Metastatic melanoma, Microcephaly, Micrognathism, Myopia, Obesity, Oropharyngeal dysphagia, Osteopenia, Otitis media, Proptosis, Strabismus, Syndromic mental retardation, x-linked, SynophrysView all (15 more) |
|
500
|
|
|
TATA-box binding protein associated factor 2 |
CIF150, MRT40, TAF2B, TAFII150 |
|
