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 |
|---|---|---|
| Congenital Hypothyroidism | causative |
mechanism: Defective Thyroid Hormone Biosynthesis
subtype: TDH5
scoped to subtype: Dyshormonogenesis
|
| Thyroid dyshormonogenesis 5 | causative germline loss of function |
mechanism: DUOXA2 Loss of Function
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.