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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

OMIM:613638

Parent Relationships

is_a chromosomal deletion syndrome

is_a autosomal dominant disease

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