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

• OMIM:615656
• ORDO:261183
• UMLS_CUI:C3180937

Ontology

Human Disease   ( DOID:0060393 )