(Q19587382)

English

autosomal dominant non-syndromic intellectual disability

non-syndromic intellectual disability characterized by an autosomal dominant inheritance pattern

autosomal dominant mental retardation
autosomal dominant non-syndromic mental retardation

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Statements

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class of disease

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non-syndromic intellectual disability

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

autosomal dominant disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

genetic intellectual disability

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genetic association

1 reference

Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation

on focus list of Wikimedia project

WikiProject Medicine

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http://purl.obolibrary.org/obo/DOID_0060307

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

http://identifiers.org/doid/DOID:0060307

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233

http://www.orpha.net/ORDO/Orphanet_178469

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Identifiers

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Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

GARD rare disease ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

Sitelinks

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Multilingual sites(0 entries)

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