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About:
syndromic intellectual disability
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
intellectual disability
label
syndromic intellectual disability
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0050888
created_by
lschriml
creation_date
2014-08-14T10:55:32Z
has_obo_namespace
disease_ontology
in_subset
DO_FlyBase_slim
http://purl.obolib...g/obo/IAO_0000115
An intellectual disability that is characterized by the presence of associated medical and behavioral sign and symptoms.
is
subClassOf
of
syndromic X-linked intellectual disability
autosomal dominant mental retardation 56
autosomal dominant mental retardation 55
neurodevelopmental disorder with midbrain and hindbrain malformations
developmental delay and seizures with or without movement abnormalities
autosomal recessive intellectual developmental disorder-72
intellectual disability-severe speech delay-mild dysmorphism syndrome
Pitt-Hopkins-like syndrome 2
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
Kaufman oculocerebrofacial syndrome
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50937795
Faceted Search & Find service v1.17_git151 as of Feb 20 2025
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