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
|