| Dataset | ClinVar Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A type of hypothyroidism that results from a defect in thyroid-stimulating hormone secretion. (Human Phenotype Ontology, HP_0008245) |
| External Link | http://www.omim.org/entry/275100 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the Secondary hypothyroidism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| TSHB | thyroid stimulating hormone, beta |
