Disease #03226 (FNEPPK1 (keratoderma, palmoplantar, nonepidermolytic, focal, type 1 (FNEPPK-1)), OMIM:613000)
| Official abbreviation |
FNEPPK1 |
| Name |
keratoderma, palmoplantar, nonepidermolytic, focal, type 1 (FNEPPK-1) |
| OMIM ID |
613000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
KRT16 |
| 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) |
|
|
