Aliases: GDF9B.
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,XX Gonadal Dysgenesis | causative germline |
mechanism: Oocyte-Granulosa Growth and Estrogen Signaling Failure
subtype: ODG2
scoped to subtype: ODG2
|
| Dermoid Cyst | untyped |
mechanism: BMP15 / H-Ras-MAPK Dysregulation in Hereditary Ovarian Teratoma
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.