Disease #01324 (EKVP1 (erythrokeratodermia variabilis et progressiva, type 1), OMIM:133200)
| Official abbreviation |
EKVP1 |
| Name |
erythrokeratodermia variabilis et progressiva, type 1 |
| OMIM ID |
133200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
18 |
| Phenotype entries for this disease |
18 |
| Associated with 3 genes |
GJA1, GJB3, GJB4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-12-07 08:45:25 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|