Disease #06703 (EKVP3 (erythrokeratodermia variabilis et progressiva, type 3), OMIM:617525)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EKVP3
Name	erythrokeratodermia variabilis et progressiva, type 3
OMIM ID	617525
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GJA1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2023-12-07 08:46:38 +01:00 (CET)

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