chromosome 19p13.13 deletion syndrome

Term ID

DOID:0060426

Synonyms

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

References

• OMIM:613638

Ontology

Human Disease   ( DOID:0060426 )