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Summary Literature (0)
MIM:601001 - EPIDERMOLYSIS BULLOSA SIMPLEX 1D, GENERALIZED, INTERMEDIATE OR SEVERE, AUTOSOMAL RECESSIVE; EBS1D


Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010976 - epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive

Disease Ontology (DO):
DOID:4644 - epidermolysis bullosa simplex