Disease #05991 (POROK1 (porokeratosis, type 1, multiple types), OMIM:175800)
| Official abbreviation |
POROK1 |
| Name |
porokeratosis, type 1, multiple types |
| OMIM ID |
175800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PMVK |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2024-05-03 20:49:53 +02:00 (CEST) |
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