Williams-Beuren syndrome

Summary
Synonym
  • Fanconi Schlesinger syndrome
  • WBS
Definition
A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23.
Super Class
autosomal dominant disease chromosomal deletion syndrome syndrome
External Links
Disease Ontology
DOID:1928
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
414 ARSD arylsulfatase D
781 CACNA2D1 calcium voltage-gated channel auxiliary subunit alpha2delta 1
Related Glycoprotein

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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: August 19, 2024