DeSanto-Shinawi syndrome

Summary
Synonym
  • Chromosome 10p12-p11 deletion syndrome
  • Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
  • Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation
  • WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome
Definition
A syndrome that is characterized by global developmental delay apparent in infancy or early childhood and associated with characteristic dysmorphic facial features, such as broad forehead, depressed nasal bridge with bulbous nasal tip, and deep-set eyes and that has_material_basis_in heterozygous mutation in the WAC gene on chromosome 10p11 or deletion at chromosome 10p12-p11.
Super Class
autosomal dominant disease syndrome
Disease Ontology
DOID:0081126
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
51322 WAC WW domain containing adaptor with coiled-coil
Displaying 1 entry
Gene ID Gene Symbol Description Source
225131 Wac WW domain containing adaptor with coiled-coil

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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