Disease #03092 (EDAID2 (dysplasia, ectodermal, and immunodeficiency, type 2), OMIM:612132)
| Official abbreviation |
EDAID2 |
| Name |
dysplasia, ectodermal, and immunodeficiency, type 2 |
| OMIM ID |
612132 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NFKBIA |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2026-02-13 08:57:52 +01:00 (CET) |
|