Disease association ontology term - MONDO:0013454 - Leber congenital amaurosis 11
Term summary
- ID
- MONDO:0013454
- Name
- Leber congenital amaurosis 11
- Ontology or CV name
- Disease association
- Definition
- Any Leber congenital amaurosis in which the cause of the disease is a mutation in the IMPDH1 gene.
