Previous symbols: FECD. Aliases: PPCD, FECD1, PPCD2.
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 |
|---|---|---|
| Posterior Polymorphous Corneal Dystrophy | unknown germline |
subtype: PPCD2
scoped to subtype: PPCD2
|
| Fuchs Endothelial Corneal Dystrophy |
untyped
Disease-causing germline mutation(s) in
|
mechanism: COL8A2 Missense Collagen VIII Dysfunction
subtype: Early-onset FECD; FECD1
scoped to subtype: FECD1
|
Identity from HGNC (snapshot 2026-10-24). Page layers are described in the gene pages documentation.