epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive

Rare Disease

MONDO:0014014

Also known as:

EBS-AR exophilin 5epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessiveepidermolysis bullosa simplex due to exophilin 5 deficiency

Genes

Clinical Trials

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Newborn Screening

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Patient Groups

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