Hyperparathyroidism 1 [Supplementary Concept]
also known as HRPT1; associated with mutations in gene HRPT2 which codes for parafibromin
Date introduced: August 24, 2012
MeSH Unique ID: C564166
Heading Mapped to:
Entry Terms:
- Parathyroid Adenoma, Familial
- Hyperparathyroidism, Familial Isolated Primary