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MIM:601001 - EPIDERMOLYSIS BULLOSA SIMPLEX 1D, GENERALIZED, INTERMEDIATE OR SEVERE, AUTOSOMAL RECESSIVE; EBS1D
Xenbase Genes:
Human Disease Resource: MIM
MONDO:0010976 - epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive |
DOID:4644 - epidermolysis bullosa simplex |