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Up to: Autosomal recessive disease · Diffuse palmoplantar keratoderma · Ectodermal dysplasia WNT10A related
Schöpf-Schulz-Passarge syndrome
A rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy.
This condition has no sub-types.