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Human Disease

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
Ontology
Human Disease   ( DOID:0060426 )
Relationships
is a type of
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Genes Involved
Zebrafish Models