(Q18553537)

English

non-syndromic intellectual disability

intellectual disability that is characterized by the absence of associated medical and behavioral signs and symptoms

nonsyndromic intellectual disability
isolated intellectual disability

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Statements

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class of disease

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intellectual disability

2 references

Monarch Disease Ontology release 2018-06-29

27 July 2018

Disease Ontology

30 November 2020

Disease Ontology ID

genetic association

1 reference

Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability.

1 reference

A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly

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WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0050889

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0050889

1 reference

Identifiers.org

https://registry.identifiers.org/registry/doid

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

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