Disease #03976 (EPKHE (Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige), OMIM:615508)

Official abbreviation	EPKHE
Name	Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige
OMIM ID	615508
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DSG1
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)

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Global Variome shared LOVD