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Human Disease

chromosome 15q11.2 deletion syndrome

Term ID
DOID:0060393
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models