Disease association ontology term - MONDO:0014732 - hypomyelinating leukodystrophy 12
Term summary
- ID
- MONDO:0014732
- Name
- hypomyelinating leukodystrophy 12
- Ontology or CV name
- Disease association
- Definition
- Any leukodystrophy in which the cause of the disease is a mutation in the VPS11 gene.
