OBO ID: DOID:0060393
Term Name: chromosome 15q11.2 deletion syndrome Search Ontology:
Synonyms:
  • 15q11.2 microdeletion syndrome
Definition: A chromosomal deletion syndrome that is characterized by intellectual disbaility, dysmorphic facies, psychiatric illness and autism spectrum disorder, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15. https://www.omim.org/entry/615656
References:
Ontology: Human Disease   ( DOID:0060393 )
OTHER chromosome 15q11.2 deletion syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None