Previous symbols: TCF8, PPCD3. Aliases: BZP, ZEB, AREB6, NIL-2-A, Zfhep, Zfhx1a, FECD6.
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 |
|---|---|---|
| Fuchs Endothelial Corneal Dystrophy |
untyped
Disease-causing germline mutation(s) in
|
mechanism: TGF-beta-Driven Endothelial-Mesenchymal Transition
|
| Posterior Polymorphous Corneal Dystrophy | untyped |
scoped to subtype: PPCD3
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.