|
101
|
|
|
T cell activation RhoGTPase activating protein |
ARHGAP47, FKSG15, IDDM21, TAGAP1 |
Asthma, Autoimmune diseases, Celiac disease, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Ileocolitis, Immune system diseases, Multiple sclerosis, Palmoplantar pustules, Psoriasis, Rheumatoid arthritis |
|
102
|
|
|
Transmembrane channel like 1 |
DFNA36, DFNB11, DFNB7 |
|
|
103
|
|
|
Twist family bHLH transcription factor 2 |
AMS, BBRSAY, DERMO1, FFDD3, SETLSS, bHLHa39 |
Ablepharon, Ablepharon macrostomia syndrome, Absent eyebrow, Alopecia, Ambiguous genitalia, Barber say syndrome, Cafe-au-lait spot, Breast aplasia, Congenital absent nipple, Congenital ectodermal dysplasia of face, Congenital epicanthus, Congenital exomphalos, Breast hypoplasia, Congenital hypoplasia of penis, Congenital omphalocele, Corneal erosion, Cryptophthalmos, Developmental delay, Ectodermal dysplasia, Ectropion, Focal facial dermal dysplasia, Hypertrichosis, Hypoplasia of nipple, Hypoplasia of the maxilla, Imperforate anus, Macrostomia, Malocclusion, Microdontia, Microtia, Mouth abnormalities, Multiple congenital anomalies, Myopia, Strabismus, Syndactyly of the toesView all (19 more) |
|
104
|
|
|
Tripartite motif containing 6 |
RNF89 |
|
|
105
|
|
|
Tripeptidyl peptidase 1 |
CLN2, GIG1, LPIC, SCAR7, TPP-1 |
Alzheimer disease, Ataxia, Cerebellar ataxia, Cerebellar atrophy, Cerebellar cortical atrophy, Cerebral atrophy, Congenital epicanthus, Developmental delay, Developmental regression, Disorder of eye, Dysarthria, Horizontal nystagmus, Mental retardation, Neuronal ceroid lipofuscinosis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Prostatic neoplasms, Prostate cancer, Seizure, Senile dementia, Speech delay, Spinocerebellar ataxiaView all (8 more) |
|
106
|
|
|
Transmembrane protein 132D |
MOLT, PPP1R153 |
|
|
107
|
|
|
Tryptophan hydroxylase 2 |
ADHD7, NTPH |
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Involutional depression, Involutional paraphrenia, Melancholia, Mental depression, Minimal brain dysfunction, Mood disorder, Paranoid schizophrenia, Psychosis, Schizophrenia |
|
108
|
|
|
Tudor domain containing 9 |
C14orf75, HIG-1, HLS, NET54, SPGF30, SPNE |
|
|
109
|
|
|
Trafficking protein particle complex subunit 6B |
NEDMEBA, TPC6 |
Brainstem atrophy, Cerebellar atrophy, Cerebral cortical atrophy, Developmental delay, Dwarfism, Hypoplasia of corpus callosum, Mental retardation, Distal hereditary motor neuronopathy, Nystagmus, Stereotyped behavior, Strabismus |
|
110
|
|
|
Tetratricopeptide repeat domain 8 |
BBS8, RP51 |
Bardet-biedl syndrome, Brachycephaly, Cataract, Ciliopathies, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Diabetes mellitus, Disorder of eye, Dwarfism, Foot polydactyly, Glaucoma, Hearing loss, Hyperinsulinism, Hypertension, Hypogonadism, Hypospadias, Impaired cognition, Keratoconus, Liver fibrosis, Age-related macular degeneration, Mental retardation, Multicystic renal dysplasia, Myopia, Nephrotic syndrome, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Polydactyly, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (21 more) |
