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Metadata
ID	DOID:0060426
Name	chromosome 19p13.13 deletion syndrome
Definition	A chromosomal deletion syndrome that has_material_basis_in a chromosome 19p13.13 deletion and that is characterized by an unusually large head size, tall stature, and intellectual disability that is usually moderate in severity. https://ghr.nlm.nih.gov/condition/19p1313-deletion-syndrome
Xrefs	MIM:613638
Parent Relationships	is_a autosomal dominant disease is_a chromosomal deletion syndrome
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance