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Disease association ontology term - MONDO:0012613 - intellectual disability, autosomal recessive 5

Term summary

ID
MONDO:0012613
Name
intellectual disability, autosomal recessive 5
Ontology or CV name
Disease association
Definition
Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the NSUN2 gene.

Parents

Annotation

Disease association

MONDO:0012613 - intellectual disability, autosomal recessive 5

References:

Genes: