Term Name: chromosome 15q11.2 deletion syndrome
Synonyms: 15q11.2 microdeletion syndrome
Definition: A chromosomal deletion syndrome that is characterized by intellectual disability, 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.
Ontology: Human Disease [DOID:0060393]   ( DOID:0060393 )

Relationships
is a type of: autosomal dominant disease chromosomal deletion syndrome