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

Official abbreviation -
Name epidermolysis bullosa, junctional, Herlitz type
OMIM ID 226700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 3 genes LAMA3, LAMB3, LAMC2
Associated tissues -
Disease features -
Remarks -

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