PomBase home

Disease association ontology term - MONDO:0013173 - intellectual disability, autosomal recessive 13

Term summary

ID
MONDO:0013173
Name
intellectual disability, autosomal recessive 13
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 TRAPPC9 gene.

Parents

Annotation

Disease association

MONDO:0013173 - intellectual disability, autosomal recessive 13

References:

Genes: