Previous symbols: PPCD. Aliases: PPD, PPCD1.
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 |
|---|---|---|
| Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome | disputed germline |
mechanism: Impaired VSX1 Transcriptional Repression; VSX1 CVC-Domain Substitution in cis with a Coding Variant
|
| Keratoconus | disputed |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.