Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Central Congenital Hypothyroidism | causative |
mechanism: Impaired Hypothalamic-Pituitary TSH Drive
|
| Isolated Thyroid-stimulating Hormone Deficiency | causative germline loss of function |
mechanism: Biallelic TSHB Loss of Function
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.