Disease association ontology term - MONDO:0010926 - familial hypocalciuric hypercalcemia 3
Term summary
- ID
- MONDO:0010926
- Name
- familial hypocalciuric hypercalcemia 3
- Ontology or CV name
- Disease association
- Definition
- Any familial hypocalciuric hypercalcemia in which the cause of the disease is a mutation in the AP2S1 gene.
