Disease association ontology term - MONDO:0013782 - pseudohypoaldosteronism type 2E
Term summary
- ID
- MONDO:0013782
- Name
- pseudohypoaldosteronism type 2E
- Ontology or CV name
- Disease association
- Definition
- Any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the CUL3 gene.
