autosomal recessive disease Schöpf-Schulz-Passarge syndrome https://github.com/monarch-initiative/mondo/issues/3293 https://github.com/monarch-initiative/mondo/issues/8538 https://www.malacards.org/card/schopf_schulz_passarge_syndrome SCHOPF-Schulz-Passarge syndrome palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome eccrine tumours with ectodermal dysplasia DOID:0111647 UMLS:C1857069 palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome eccrine tumors-ectodermal dysplasia SSPS A rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy. keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome Orphanet:50944 MONDO:0009145 MESH:C565607 MEDGEN:347366 ICD9:758.89 SCTID:700062000 GARD:0016649 OMIM:224750 diffuse palmoplantar keratoderma ectodermal dysplasia WNT10A related