|
371
|
|
|
Thrombospondin type laminin G domain and EAR repeats |
C21orf29, DFNB98, ECTD14, STHAG10, TSP-EAR |
Alopecia, Colorectal cancer, Deafness, Dyskinetic syndrome, Ectodermal dysplasia, Hearing loss, Hypodontia, Impaired cognition, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Peg-shaped teeth, Sagittal craniosynostosis, Taurodontism |
|
372
|
|
|
Toll like receptor 9 |
CD289 |
|
|
373
|
|
|
Triggering receptor expressed on myeloid cells 2 |
AD17, PLOSL2, TREM-2, Trem2a, Trem2b, Trem2c |
Abulia, Agnosia, Alexia, Alzheimer disease, Amyotrophic lateral sclerosis, Anomia, Anxiety disorder, Aphasia, Apraxia, Behavioral variant of frontotemporal dementia, Brain atrophy, Broca aphasia, Cerebral atrophy, Cerebral cortical atrophy, Compulsive hoarding, Dementia, Dementia of frontal lobe, Developmental regression, Dyscalculia, Dysgraphia, Dyslexia, Dysphasia, Frontotemporal cerebral atrophy, Frontotemporal dementia, Grammar-specific speech disorder, Hallucinations, Hydrocephalus, Language disorders, Laryngospasm, Leukemia, Mental depression, Mental retardation, Mood swings, Nasu-hakola disease, Oculomotor apraxia, Oculovestibuloauditory syndrome, Osteochondrodysplasia, Parkinson disease, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, Nonfluent aphasia, Progressive non-fluent aphasia, Psychosis, Respiratory failure, Seizure, Semantic dementia, Senile dementia, Senile paranoid dementia, Senile plaques, Skeletal dysplasia, Speech disorders, Stereotyped behavior, Temporal cortical atrophyView all (37 more) |
|
374
|
|
|
Triggering receptor expressed on myeloid cells 1 |
CD354, TREM-1 |
|
|
375
|
|
|
TERF2 interacting protein |
DRIP5, RAP1 |
|
|
376
|
|
|
Toll interacting protein |
IL-1RAcPIP |
|
|
377
|
|
|
Transmembrane and coiled-coil domains 1 |
CFSMR1, HP10122, PCIA3, PNAS-136, TMCC4 |
Accessory nipple, Atrial septal defect, Autism, Bone disease, Brachycephaly, Cerebral cortical atrophy, Cerebrofaciothoracic dysplasia, Cleft palate and bilateral cleft lip, Renal agenesis, Congenital epicanthus, Rib fusion, Congenital musculoskeletal anomalies, Cryptorchidism, Developmental delay, Dwarfism, Dysmorphic features, Glaucoma, Hearing loss, High palate, Hypoplasia of corpus callosum, Hypoplasia of the maxilla, Impaired cognition, Mental retardation, Macrocephaly, Macrostomia, Micrognathism, Motor delay, Multiple congenital anomalies, Hypotonia, Odontome, Periventricular leukomalacia, Poliosis, Posteriorly rotated ear, Pulmonary stenosis, Renal aplasia, Scoliosis, Open angle glaucoma, Sprengel deformity, Strabismus, Synophrys, Postaxial hand polydactyly, UranostaphyloschisisView all (27 more) |
|
378
|
|
|
Transmembrane protein 106B |
HLD16 |
Abulia, Alexia, Anomia, Anxiety disorder, Aphasia, Apraxia, Behavioral variant of frontotemporal dementia, Brain atrophy, Broca aphasia, Cerebral atrophy, Compulsive hoarding, Coronary artery disease, Dementia, Dysarthria, Dyscalculia, Dysgraphia, Dyslexia, Dysphasia, Frontotemporal cerebral atrophy, Frontotemporal dementia, Grammar-specific speech disorder, Hypomyelinating leukodystrophy, Hypoplasia of corpus callosum, Leukodystrophy, Mental depression, Mood disorder, Nystagmus, Parkinson disease, Nonfluent aphasia, Progressive non-fluent aphasia, Psychosis, Seizure, Semantic dementia, Senile plaques, Stereotyped behavior, Temporal cortical atrophyView all (21 more) |
|
379
|
|
|
Tripartite motif containing 44 |
AN3, DIPB, HSA249128, MC7 |
|
|
380
|
|
|
Tet methylcytosine dioxygenase 2 |
IMD75, KIAA1546, MDS |
Agranulocytosis, Anemia, Anemia with ringed sideroblasts, Angioimmunoblastic t-cell lymphoma, Anorexia, Breast cancer, Breast carcinoma, Budd-chiari syndrome, Chromophobe carcinoma, Chronic obstructive pulmonary disease, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Congestive heart failure, Dysplastic granulopoesis, Eosinophilia, Erythroid hypoplasia, Hemangioma, Hematologic neoplasms, Hypertension, Hypochromic anemia, Inflammatory bowel disease, Leukemia, Non-hodgkin lymphoma, Mastocytosis, Melanoma, Multiple lineage myelodysplasia, Multiple sclerosis, Myelodysplasia, Myelodysplastic syndrome, Myelofibrosis, Myeloid leukemia, Myeloid leukemia with multilineage dysplasia, Myelomonocytic leukemia, Myocardial infarction, Neutropenia, Pancytopenia, Papillary renal carcinoma, Polycythemia vera, Portal hypertension, Portal vein thrombosis, Promyelocytic leukemia, Prostatic neoplasms, Prostate cancer, Renal carcinoma, Schizophrenia, Sezary syndrome, Single lineage myelodysplasia, Stroke, Systemic mastocytosis, Systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease, Systemic mastocytosis with associated hematologic neoplasm, T-cell lymphoma, Thrombocythemia, Thrombocytosis, Transient ischemic attack, Ulcerative colitisView all (43 more) |
