Previous symbols: WDR69. Aliases: FLJ25955, ODA16, DNAAF18.
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 |
|---|---|---|
| Primary_Ciliary_Dyskinesia |
untyped
Limited evidence for PCD association
|
|
| Visceral heterotaxy |
untyped
Pathogenic Variants
|
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 |
|---|---|---|---|
| primary ciliary dyskinesia MONDO:0016575 | AR | Limited 2024-06-13 |
Primary_Ciliary_Dyskinesia
untyped
|
| visceral heterotaxy MONDO:0018677 | AR | Moderate 2024-07-11 |
Congenital Heart Disease
not named
Visceral heterotaxy
untyped
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.