About: Prieto syndrome

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	syndromic X-linked intellectual disability X-linked recessive disease nodeID://b50939433
label	Prieto syndrome
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060805
database_cross_reference	OMIM:309610 ORDO:2958
has_exact_synonym	Prieto-Badia-Mulas syndrome (en) X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A syndromic X-linked intellectual disability characterized by intellectual disability, facial dysmorphism, patella luxation, clinodactyly, subcortical cerebral atrophy, and abnormal growth of the teeth that has_material_basis_in variation in the chromosome region Xp11-q21.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50939434

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