About: chromosome 19p13.13 deletion syndrome

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An Entity of Type : owl:Class, within Data Space : demo.openlinksw.com associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease chromosomal deletion syndrome nodeID://b50938820
label	chromosome 19p13.13 deletion syndrome
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060426
created_by	elvira
creation_date	2015-09-29T15:26:36Z
database_cross_reference	OMIM:613638
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	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.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50938821

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