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Metadata
ID	DOID:0060389
Name	chromosome 10q23 deletion syndrome
Definition	A chromosomal deletion syndrome that is characterized by dysmorphic facies, developmental delay and multiple congenital abnormalities and huvenile polyposis, has_material_basis_in recurrent deletions of chromosome 10q22.3-q23.2. https://pubmed.ncbi.nlm.nih.gov/21248748
Xrefs	MESH:C567385 OMIM:612242
Parent Relationships	is_a chromosomal deletion syndrome