Disease #02335 (Epidermolysis bullosa simplex, autosomal recessive, OMIM:601001)

MyGenome LOVD - This database is for training purposes only

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

Official abbreviation	-
Name	Epidermolysis bullosa simplex, autosomal recessive
OMIM ID	601001
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	KRT14, KRT5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A