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MIM:604536 - ECTODERMAL DYSPLASIA/SKIN FRAGILITY SYNDROME; EDSFS
Xenbase Genes: pkp1
Human Disease Resource: MIM
MONDO:0011472 - epidermolysis bullosa simplex due to plakophilin deficiency |
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MONDO:0011472 - epidermolysis bullosa simplex due to plakophilin deficiency |