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521
|
|
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T-box transcription factor 2 |
VETD |
Atrial septal defect, Autism, Brachycephaly, Congenital anomaly of eye, Aplasia of the thymus, Congenital camptodactyly, Congenital epicanthus, Rib fusion, Congenital pectus carinatum, Developmental delay, Double outlet right ventricle, Dwarfism, Ectopic pupil, Glabellar hemangioma, Hashimoto disease, Hypertension, Hypoparathyroidism, Isolated somatotropin deficiency, Klippel feil syndrome, Neck webbing, Neuroblastoma, Patent ductus arteriosus, Pulmonary stenosis, Scoliosis, Somatotropin deficiency, Sprengel deformity, Thyroiditis, Vertebral anomalies and variable endocrine and t-cell dysfunctionView all (13 more) |
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522
|
|
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T-box transcription factor 5 |
HOS |
Aortic valve disease, Atrial fibrillation, Atrial septal defect, Atrioventricular block, Atrioventricular septal defect, Clinodactyly, Short clavicles, Congenital pectus excavatum, Holt-oram syndrome, Hypoplastic left heart syndrome, Paroxysmal atrial fibrillation, Patent ductus arteriosus, Phocomelia, Polydactyly, Pulmonary venous return anomaly, Radioulnar synostosis, Scoliosis, Secundum atrial septal defect, Sprengel deformity, Syndactyly of fingers, Thumb aplasia, Ventricular septal defect, Wildervanck`s syndromeView all (8 more) |
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523
|
|
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T-box transcription factor 6 |
SCDO5 |
|
|
524
|
|
|
T-box transcription factor 15 |
TBX14 |
Alopecia, Alopecia, male pattern, Ambiguous genitalia, Androgenetic alopecia, Blepharophimosis, Brachydactyly, Camptodactyly of fingers, Congenital camptodactyly, Congenital clubfoot, Dislocated radial head, Developmental dysplasia of the hip, Short femur, Dwarfism, Elbow flexion contracture, Flexion contracture of wrist, Frontal bossing, Hydranencephaly, Hydrocephalus, Hydronephrosis, Macrocephaly, Mesomelia, Microcornea, Microglossia, Micrognathism, Microphthalmos, Pelviscapular dysplasia, Ramer ladda syndrome, Rhizomelia, Stenosis of external auditory canal, Strabismus, Syndactyly of the toesView all (16 more) |
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525
|
|
|
Thromboxane A2 receptor |
BDPLT13, TXA2-R |
|
|
526
|
|
|
Thromboxane A synthase 1 |
BDPLT14, CYP5, CYP5A1, GHOSAL, THAS, TS, TXAS, TXS |
Anemia, Breast cancer, Diaphyseal dysplasia, Ghosal hematodiaphyseal dysplasia, Osteosclerosis, Myelofibrosis, Prostatic neoplasms, Prostate cancer, Schizophrenia, Speech disorders, Thromboxane synthetase deficiency |
|
527
|
|
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Transcription elongation factor A2 |
TFIIS |
|
|
528
|
|
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Transcription factor 4 |
CDG2T, E2-2, FCD2, FECD3, ITF-2, ITF2, PTHS, SEF-2, SEF2, SEF2-1, SEF2-1A, SEF2-1B, SEF2-1D, TCF-4, bHLHb19 |
Accessory nipple, Alopecia, Amyotrophy, Aphasia, Astigmatism, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Brachycephaly, Celiac disease, Cholangiocarcinoma, Cholangitis, Cholelithiasis, Cirrhosis, Clinodactyly, Clonic seizures, Colorectal cancer, Congenital epicanthus, Congenital microcephaly, Congestive heart failure, Corneal endothelial dystrophy, Cryptorchidism, Development disorder, Developmental delay, Diabetes mellitus, Dysautonomia, Dysmorphic features, Dysphasia, Epileptic encephalopathy, Eosinophilia, Fuchs endothelial dystrophy, Neoplasm of gallbladder, Gastroesophageal reflux disease, Heart diseases, Hiatal hernia, Hirschsprung disease, Hodgkin disease, Hypoalbuminemia, Hypoplasia of corpus callosum, Hypotonic seizures, Mental retardation, Jacksonian seizure, Liver neoplasms, Liver cancer, Liver carcinoma, Liver failure, Liver fibrosis, Macrostomia, Mental depression, Microcephaly, Microlissencephaly, Mood disorder, Motor delay, Movement disorders, Myopia, Nervous system diseases, Neurodevelopmental disorders, Non-syndromic intellectual disability, Nonorganic psychosis, Osteopenia, Osteoporosis, Pancreatitis, Paranoia, Penis agenesis, Pitt-hopkins syndrome, Pleural effusion, Portal hypertension, Prostate cancer, Prostate cancer, hereditary, Psychosis, Renal insufficiency, Schizophrenia, Sclerosing cholangitis, Scoliosis, Seizure, Sleep apnea, Specific learning disorder, Spider hemangioma, Strabismus, Thyroiditis, Ulcerative colitis, UveitisView all (67 more) |
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529
|
|
|
T-box transcription factor 3 |
TBX3-ISO, UMS, XHL |
Benign prostatic hyperplasia, Breast adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Breast aplasia, Congenital anomaly of limb, Breast hypoplasia, Short clavicles, Congenital hypoplasia of penis, Congenital hypoplasia of radius, Congenital pectus carinatum, Cryptorchidism, Dwarfism, Ectopic anus, Gastric cancer, Hernia of abdominal wall, Hypodontia, Hypoplasia of nipple, Imperforate anus, Laryngomalacia, Marfan syndrome, Obesity, Odontome, Penis agenesis, Polydactyly, Prostatic neoplasms, Prostate cancer, Renal hypoplasia, Sprengel deformity, Stomach neoplasms, Stroke, Thyroid diseases, Postaxial hand polydactyly, Ulnar-mammary syndrome, Uterine anomalies, Ventricular septal defectView all (25 more) |
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530
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|
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Transcription factor 3 |
AGM8, AGM8A, AGM8B, E2A, E47, ITF1, TCF-3, VDIR, bHLHb21, p75 |
African burkitt`s lymphoma, Agammaglobulinemia, Arthritis, Bipolar disorder, Bronchiectasis, Burkitt`s lymphoma, Colorectal cancer, Congenital epicanthus, Conjunctivitis, High palate, Hodgkin disease, Hypogammaglobulinemia, Immunologic deficiency syndromes, Lymphoblastic leukemia, Malabsorption syndrome, Neutropenia, Osteomyelitis, Otitis media, Immunodeficiency, SinusitisView all (5 more) |
