About: X-linked intellectual developmental disorder 109

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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	syndromic X-linked intellectual disability X-linked recessive disease nodeID://b50941965
label	X-linked intellectual developmental disorder 109 (en)
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0080984
database_cross_reference	GARD:2378 OMIM:309548 ORDO:100973
has_exact_synonym	Fragile XE syndrome fragile site on chromosome Xq28
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A syndromic X-linked intellectual disability characterized by mildly to moderately impaired intellectual development associated with learning difficulties, communication deficits, attention problems, hyperactivity, and autistic behavior and that has_material_basis_in disruption of the FMR2 gene (AFF2, either by expansion of a CCG repeat in the 5-prime untranslated region or by deletion.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50941966

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