Disease association ontology term - MONDO:0009796 - ornithine aminotransferase deficiency
Term summary
- ID
- MONDO:0009796
- Name
- ornithine aminotransferase deficiency
- Ontology or CV name
- Disease association
- Definition
- A very rare inherited retinal dystrophy characterized by progressive chorioretinal atrophy, myopia and early cataract.
