Aliases: RALDH2.
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 |
|---|---|---|
| Congenital Diaphragmatic Hernia | no genetic record |
mechanism: Retinoid Signaling and Pleuroperitoneal Fold Mesenchymal Deficit
|
| Fetal Alcohol Spectrum Disorder | no genetic record |
mechanism: Competition for Retinaldehyde Dehydrogenase Activity
animal model: Xenopus ethanol-exposed gastrula with RALDH manipulation
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.