Previous symbols: PMX1. Aliases: PHOX1.
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 |
|---|---|---|
| Agnathia-Otocephaly Complex | causative |
mechanism: PRRX1 Loss of Function
animal model: Mouse (Mus musculus)
|
| Aortic Valve Stenosis | susceptibility |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.