Disease association ontology term - MONDO:0010398 - syndromic X-linked intellectual disability 14
Term summary
- ID
- MONDO:0010398
- Name
- syndromic X-linked intellectual disability 14
- Ontology or CV name
- Disease association
- Definition
- Any X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the UPF3B gene.
