Disease association ontology term - MONDO:0018100 - familial primary hypomagnesemia
Term summary
- ID
- MONDO:0018100
- Name
- familial primary hypomagnesemia
- Ontology or CV name
- Disease association
- Definition
- A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration.
