Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive

MONDO:0010976

A basal subtype of epidermolysis bullosa simplex EBS characterized by generalized or, less frequently, localized acral blistering.

Also known as: EBS, autosomal recessive K14, EBS-AR KRT14, KRT14-related autosomal recessive EBS, KRT14-related autosomal recessive epidermolysis bullosa simplex, KRT14-related epidermolysis bullosa simplex, epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive, epidermolysis bullosa simplex, autosomal recessive type 1, EBSB1

1 clinical trial for this condition and its sub-types, 0 tagged with Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive itself.

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↑ Epidermolysis bullosa simplex (6)

Including sub-types (1) Tagged with Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive (0)

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