Aliases: P138-TOX, P138(TOX), THOX2, LNOX2.
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: TDH6
computational model: Minimal Hypothalamic-Pituitary-Thyroid Feedback Model
scoped to subtype: Dyshormonogenesis
|
| Familial Nonmedullary Thyroid Carcinoma | disputed germline |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.