Aliases: PRDM19, FOG2, hFOG-2, ZNF89B.
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 partial gonadal dysgenesis | unknown germline | |
| Congenital Diaphragmatic Hernia | causative | |
| Holt-Oram syndrome | no genetic record |
mechanism: Cofactor and Chromatin Remodeling Dysfunction
|
An entry matches when ClinGen's MONDO disease is the entry's own disease term, a subtype term, or an exact-match mapping. An amber status marks an entry ClinGen supports the gene for (Definitive, Strong or Moderate) whose own record does not type it. A Limited, Disputed or Refuted tier on such an entry is not a gap.
| ClinGen disease | MOI | Classification | dismech entry |
|---|---|---|---|
| congenital heart disease MONDO:0005453 | AD | Limited 2026-07-07 |
Congenital Heart Disease
not named
|
| diaphragmatic hernia 3 MONDO:0012431 | AD | Definitive 2026-08-04 |
no dismech entry |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.