Previous symbols: FKHL5. Aliases: FREAC1.
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 |
|---|---|---|
| Alveolar capillary dysplasia with misalignment of pulmonary veins | causative |
mechanism: FOXF1 Coding or Upstream Enhancer Lesion
|
| Esophageal Atresia | susceptibility | |
| Gastroesophageal Reflux Disease |
untyped
Risk Factor
|
|
| Laryngotracheoesophageal Cleft |
untyped
Associated
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.