|
681
|
|
|
Thyrotropin releasing hormone |
Pro-TRH, TRF |
Amnesia, Catalepsy, Clonic seizures, Coma, Dwarfism, Endometrioma, Endometriosis, Hypertension, Hypothalamic hypothyroidism, Hypotonic seizures, Isolated thyrotropin-releasing hormone deficiency, Jacksonian seizure, Learning disorders, Leukemia, Mental depression, Mental retardation, Myeloid leukemia, Narcolepsy, Narcolepsy-cataplexy syndrome, Narcosis, Respiratory failure, Seizure, StuporView all (8 more) |
|
682
|
|
|
Thyrotropin releasing hormone receptor |
CHNG7, TRH-R |
Central hypothyroidism, Congenital central hypothyroidism, Congenital exomphalos, Developmental delay, Dyssomnia, Hypothyroidism, Macroglossia, Resistance to thyrotropin-releasing hormone syndrome, Sleep disorders, Thyroid hormone resistance, Thyrotropin-releasing hormone resistance |
|
683
|
|
|
Trio Rho guanine nucleotide exchange factor |
ARHGEF23, MEBAS, MRD44, MRD63, tgat |
Atrioventricular septal defect, Attention deficit hyperactivity disorder, Autism, Brachydactyly, Camptodactyly of fingers, Clinodactyly, Congenital epicanthus, Congenital microcephaly, Congenital pectus excavatum, Congenital ptosis, Coronary heart disease, Deafness, Developmental delay, Dysmorphic features, Dyssomnia, High palate, Hypercalcemia, Hypodontia, Leukemia, Liver neoplasms, Liver cancer, Macrotia, Mental depression, Mental retardation, Metastatic melanoma, Microcephaly, Micrognathism, Motor delay, Multiple congenital anomalies, Myeloid leukemia, Neurodevelopmental disorders, Obsessive-compulsive disorder, Scoliosis, Sleep disorders, Specific learning disorder, Stereotyped behavior, Strabismus, Syndactyly of the toes, Synophrys, Thyroid hormone resistanceView all (25 more) |
|
684
|
|
|
Transient receptor potential cation channel subfamily C member 3 |
SCA41, TRP3 |
|
|
685
|
|
|
Transient receptor potential cation channel subfamily C member 4 |
HTRP-4, HTRP4, TRP4 |
|
|
686
|
|
|
Transient receptor potential cation channel subfamily C member 5 |
PPP1R159, TRP5 |
|
|
687
|
|
|
Transient receptor potential cation channel subfamily C member 6 |
FSGS2, TRP6 |
Behavior disorders, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glomerular hyalinosis, Glomerulosclerosis, Hypertension, Kidney disease, Kidney failure, Mental disorders, Nephritis, Nephrotic syndrome, Renal glomerular diseaseView all (1 more) |
|
688
|
|
|
Transient receptor potential cation channel subfamily M member 2 |
EREG1, KNP3, LTRPC2, LTrpC-2, NUDT9H, NUDT9L1, TRPC7 |
|
|
689
|
|
|
Transcriptional repressor GATA binding 1 |
GC79, LGCR |
Alopecia, Alopecia areata, Anaplastic carcinoma, Arthritis, Atresia of nasolacrimal duct, Autism, Avascular necrosis of the capital femoral epiphysis, Basal cell neoplasm, Bone disease, Brachydactyly, Breast carcinoma, Camptodactyly of fingers, Carcinoma, Congenital clubfoot, Congenital diaphragmatic hernia, Congenital pectus carinatum, Coxa magna, Craniosynostosis, Developmental delay, Diverticular diseases, Drachtman weinblatt sitarz syndrome, Dwarfism, Dysmorphic features, Frontal bossing, Hearing loss, High palate, Langer-giedion syndrome, Legg-calve-perthes disease, Macrocephaly, Macrotia, Mental retardation, Microcephaly, Microdontia, Micrognathism, Mitral valve prolapse, Multiple congenital anomalies, Osteopenia, Rheumatoid arthritis, Scoliosis, Skin carcinoma, Talipes, Trichorhinophalangeal dysplasia, Vesicoureteral refluxView all (28 more) |
|
690
|
|
|
TSC complex subunit 1 |
LAM, TSC |
Action myoclonus-renal failure syndrome, Adenoma sebaceum, Angiofibroma, Angiomyolipoma of kidney, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Benign neoplasm of bladder, Urinary bladder cancer, Bladder neoplasm, Bladder carcinoma, Cafe-au-lait spot, Carcinoma, Cardiac rhabdomyoma, Chordoma, Chromophobe carcinoma, Chylopericardium, Ciliopathies, Clonic seizures, Cognitive disorder, Congenital coloboma of iris, Congenital macrodactylia, Congestive heart failure, Cortical dysplasia, Cryptogenic west syndrome, Dentatorubral pallidoluysian atrophy, Developmental delay, Dyscognitive seizures, Ependymoma, Epilepsy, Epileptic encephalopathy, Focal cortical dysplasia, Gingivitis, Hemimegalencephaly, Hydrocephalus, Hypothyroidism, Hypotonic seizures, Impaired cognition, Inclusion-body disease, Isolated focal cortical dysplasia, Jackknife seizures, Jacksonian seizure, Liver carcinoma, Lymphangiomyomatosis, May-white syndrome, Mental retardation, Mouth neoplasms, Malignant neoplasm of mouth, Multiple renal cysts, Myoclonic epilepsy, Optic atrophy, Optic nerve glioma, Pancreatic neoplasm, Papillary renal carcinoma, Periungual fibroma, Phakomatosis pigmentovascularis, Precocious puberty, Pulmonary lymphangiomyomatosis, Renal carcinoma, Renal cyst, Renal insufficiency, Retinal hamartoma, Salaam seizures, Seizure, Shagreen patch, Spasmus nutans, Specific learning disorder, Symptomatic west syndrome, Tuberous sclerosis, West syndrome, Wolff-parkinson-white syndromeView all (56 more) |
