Disease association ontology term - MONDO:0012056 - Leber congenital amaurosis 9
Term summary
- ID
- MONDO:0012056
- Name
- Leber congenital amaurosis 9
- Ontology or CV name
- Disease association
- Definition
- Any Leber congenital amaurosis in which the cause of the disease is a mutation in the NMNAT1 gene.
