|
871
|
|
|
Transmembrane protein 259 |
ASBABP1, C19orf6, MBRL, MEMBRALIN, R32184_3 |
|
|
872
|
|
|
Tudor domain containing 12 |
ECAT8 |
|
|
873
|
|
|
Thymosin beta 10 |
MIG12, TB10 |
|
|
874
|
|
|
T cell immunoglobulin and mucin domain containing 4 |
SMUCKLER, TIM4 |
|
|
875
|
|
|
Transmembrane protein 132C |
PPP1R152 |
|
|
876
|
|
|
Translocase of inner mitochondrial membrane 50 |
MGCA9, TIM50, TIM50L |
3-methylglutaconic aciduria, Brain atrophy, Cerebral atrophy, Developmental delay, Epileptic encephalopathy, Infantile spasms, Mental retardation, Mitochondrial encephalopathy, Hypotonia, Optic atrophy, Status epilepticus |
|
877
|
|
|
Thyroid hormone receptor interactor 13 |
16E1BP, MVA3, OOMD9, OZEMA9 |
Ambiguous genitalia, Aniridia, Aortic coarctation, Aortic valve insufficiency, Atrial septal defect, Cafe-au-lait spot, Camptodactyly of fingers, Neoplasm, Cataract, Colonic neoplasms, Congenital epicanthus, Dandy-walker syndrome, Developmental delay, Duodenal atresia, Dwarfism, Embryonal neoplasm, Frontal bossing, Tumor, Glaucoma, Holoprosencephaly, Hypertension, Hypothyroidism, Intestinal polyposis, Liver neoplasms, Liver carcinoma, Lung neoplasms, Lymphoblastic leukemia, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Mosaic variegated aneuploidy, Multicystic renal dysplasia, Muscular dystrophy, Myelodysplasia, Myelodysplastic syndrome, Nephroblastoma, Rhabdomyosarcoma, Stomach neoplasms, Subaortic stenosis, Vaginal neoplasms, Wilms tumorView all (27 more) |
|
878
|
|
|
Thyroid hormone receptor interactor 12 |
MRD49, TRIP-12, TRIPC, ULF |
Atrial septal defect, Autism spectrum disorder, Autism, Clinodactyly, Congenital epicanthus, Developmental delay, Dysmorphic features, High palate, Mental retardation, Macrostomia, Meconium ileus, Micrognathism, Neurodevelopmental disorders, Strabismus, Trigonocephaly |
|
879
|
|
|
Thyroid hormone receptor interactor 11 |
ACG1A, CEV14, GMAP-210, GMAP210, ODCD, ODCD1, TRIP-11, TRIP230 |
Achondrogenesis, Acromelia, Brachydactyly, Congenital exomphalos, Congenital genu recurvatum, Short clavicles, Congenital hypoplasia of radius, Congenital pectus carinatum, Defect of skull ossification, Dentinogenesis imperfecta, Developmental delay, Dwarfism, Frontal bossing, Hernia, femoral, Hydrops fetalis, Hypertension, Hypoplasia of lower limb, Cystic hygroma, Macrocephaly, Mesomelia, Micrognathism, Micromelia, Motor delay, Hypoglycemia, Hypotonia, Odontochondrodysplasia, Osteochondrodysplasia, Osteoporosis, Patent ductus arteriosus, Polycystic kidney disease, Pyle metaphyseal dysplasia, Rhizomelia, Scoliosis, Skeletal dysplasia, Spondylometaphyseal dysplasia with dentinogenesis imperfecta, Strabismus, Strudwick syndrome, Thoracic hypoplasiaView all (23 more) |
|
880
|
|
|
Thyroid hormone receptor interactor 4 |
ASC-1, ASC1, HsT17391, MDCDC, SMABF1, ZC2HC5 |
Alzheimer disease, Amyotrophy, Arthrogryposis multiplex congenita, Congenital alveolar dysplasia, Cardiomyopathy, Pulmonary hypoplasia, Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Diaphragmatic eventration, Dysphagia, Gastroesophageal reflux disease, High palate, Hypohidrosis, Microstomia, Minicore myopathy with external ophthalmoplegia, Motor delay, Muscular dystrophy, Muscular dystrophy, congenital, Patent ductus arteriosus, Peripheral axonal neuropathy, Phrynoderma, Scoliosis, Spinal muscular atrophy, Spinal muscular atrophy with congenital bone fracturesView all (11 more) |
