Previous symbols: CHED2, CDPD1. Aliases: dJ794I6.2, BTR1, NaBC1, FECD4.
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
|
|
| Corneal Dystrophy | no genetic record |
mechanism: Corneal Endothelial Sodium-Borate Cotransport Failure; Layer-Restricted Corneal Deposition or Cellular Failure
subtype: CHED
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.