Disease #01776 (epidermolysis bullosa, junctional, Herlitz type, OMIM:226700)

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	Curator: Johan T. den Dunnen

Official abbreviation	-
Name	epidermolysis bullosa, junctional, Herlitz type
OMIM ID	226700
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	LAMA3, LAMB3, LAMC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A