Aliases: HHG-3, MGC35145.
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 |
|---|---|---|
| 46,XY complete gonadal dysgenesis | causative germline |
mechanism: DHH paracrine signaling failure
subtype: DHH-related nonsyndromic complete gonadal dysgenesis
|
| 46,XY partial gonadal dysgenesis | causative germline |
mechanism: Biallelic DHH sequence alteration; Impaired Leydig-cell maturation
subtype: DHH-related PGD
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.