Disease #01379 (EPPK (keratoderma, palmoplantar, epidermolytic (EPPK)), OMIM:144200)
| Official abbreviation |
EPPK |
| Name |
keratoderma, palmoplantar, epidermolytic (EPPK) |
| OMIM ID |
144200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
79 |
| Phenotype entries for this disease |
79 |
| Associated with 2 genes |
KRT1, KRT9 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|