Aliases: FETUA, A2HS, HSGA.
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 |
|---|---|---|
| Alopecia-Intellectual Disability Syndrome 1 | causative germline |
mechanism: Biallelic AHSG Missense Variant
animal model: Ahsg-null mouse
|
| Otosclerosis | no genetic record |
mechanism: Dysregulated TGF-beta Signaling in the Otic Capsule
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.