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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 21/09/07 |
| Symbol | TRHD | |||
| Location | 3q13.3-q21 | |||
| Name | thyrotropin releasing hormone deficiency | |||
| Corresponding gene | TRH | |||
| Main clinical features | isolated central hypothyroidism, with dysfunction of hypothalamic TRH release | |||
Genetic determination
| Function/system disorder
| endocrinology | Type
| disease
| |
| Gene product |
| Name | thyrotropin releasing hormone (TRH), major hypothalamic mediator of release of TSHB |