familial primary hyperparathyroidism
MONDO:0016365Mondo
Findings
No curated finding names familial primary hyperparathyroidism yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of primary hyperparathyroidism (disease) that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0016365), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
1 name
Resolves to: familial primary hyperparathyroidism
- Also called
- hereditary primary hyperparathyroidism (disease)