Schopf-Schulz-Passarge syndrome

Summary
Synonym
  • SSPS
  • 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
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.
Super Class
autosomal dominant disease ectodermal dysplasia
Disease Ontology
DOID:0111647
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
80326 WNT10A Wnt family member 10A
Displaying 1 entry
Gene ID Gene Symbol Description Source
22409 Wnt10a wingless-type MMTV integration site family, member 10A
Displaying 1 entry
Gene ID Gene Symbol Description Source
171994 lin-44 Abnormal cell lineage protein 44

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024