Aliases: WNT-4.
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 |
|---|---|---|
| Mullerian Aplasia and Hyperandrogenism | causative |
mechanism: Heterozygous WNT4 Loss of Function
|
| Pelvic Organ Prolapse | susceptibility | |
| Endometriosis |
untyped
Risk Factor
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.