obsolete_Schöpf-Schulz-Passarge syndrome true 3.88.0 OMIM:224750 ICD10:Q82.8 Palmoplantar keratoderma - cystic eyelids - hypodontia - hypotrichosis orphanet http://purl.obolibrary.org/obo/MONDO_0009145 Keratosis palmoplantaris - cystic eyelids - hypodontia - hypotrichosis 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. Palmoplantar hyperkeratosis - cystic eyelids - hypodontia - hypotrichosis Eccrine tumors-ectodermal dysplasia SSPS Replaced by Mondo term MONDO_0009145, with which this term was previously merged. This term is an old static import into EFO and is therefore out of date. It is being obsoleted in EFO for preservation and tracking. This term should be considered obsolete in EFO only if it differs from the domain source. Replaced by: http://purl.obolibrary.org/obo/MONDO_0009145