Preferred Label : Schöpf-Schulz-Passarge syndrome;
ICD-11 definition : Schöpf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia
characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma,
hypotrichosis, hypodontia and nail dystrophy.;
Origin ID : 441760957;
Currated CISMeF NLP mapping
Schöpf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia
characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma,
hypotrichosis, hypodontia and nail dystrophy.
