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Disease Ontology Browser
Schopf-Schulz-Passarge syndrome (DOID:0111647)
Alliance: disease page
Synonyms: eccrine tumors-ectodermal dysplasia; keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome; palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome; palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome; SSPS
Alt IDs: OMIM:224750, MESH:C565607, ORDO:50944, UMLS_CUI:C1857069
Definition: An ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WNT10A gene on chromosome 2q35.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory