Previous symbols: ED1, EDA2, ODT1. Aliases: EDA1, XLHED, HED, XHED, ED1-A1, ED1-A2, EDA-A1, EDA-A2.
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 |
|---|---|---|
| X-linked Hypohidrotic Ectodermal Dysplasia | causative |
mechanism: EDA Ligand Deficiency
animal model: Mouse (Mus musculus)
|
| Tooth Agenesis |
untyped
Pathogenic Variants
|
mechanism: EDA-EDAR-NF-kappaB Signaling Deficiency
subtype: EDA-related
scoped to subtype: EDA-related
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.