Disease association ontology term - MONDO:0013805 - intellectual disability, autosomal dominant 13
Term summary
- ID
- MONDO:0013805
- Name
- intellectual disability, autosomal dominant 13
- Ontology or CV name
- Disease association
- Definition
- Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene.
