About: distal 10q 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	chromosomal deletion syndrome
label	distal 10q deletion syndrome
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060390
created_by	elvira
creation_date	2015-09-28T16:08:42Z
database_cross_reference	ICD10CM:Q93.5 MESH:C567182 OMIM:609625 ORDO:96148
has_exact_synonym	chromosome 10q26 deletion syndrome (en) distal monosomy 10q (en) monosomy 10qter (en) telomeric deletion 10q (en) terminal chromosome 10q26 deletion syndrome (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	A chromosomal deletion syndrome that is characterized by developmental delay, intellectual disability, behavioral problems and facial facies caused by a missing copy of the long arm of chromosome 10.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50938765

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