Disease association ontology term - MONDO:0014872 - congenital stationary night blindness 1H
Term summary
- ID
- MONDO:0014872
- Name
- congenital stationary night blindness 1H
- Ontology or CV name
- Disease association
- Definition
- Any congenital stationary night blindness in which the cause of the disease is a mutation in the GNB3 gene.
