Disease association ontology term - MONDO:0014169 - dyschromatosis universalis hereditaria 3
Term summary
- ID
- MONDO:0014169
- Name
- dyschromatosis universalis hereditaria 3
- Ontology or CV name
- Disease association
- Definition
- Any dyschromatosis universalis hereditaria in which the cause of the disease is a mutation in the ABCB6 gene.
