MeSH Browser

MeSH Supplementary: Hyperparathyroidism 1
Unique ID: C564166
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564166
Entry Term(s): Hyperparathyroidism, Familial Isolated Primary; Parathyroid Adenoma, Familial
Registry Number: 0
Heading Mapped to: *Hyperparathyroidism, Primary
Frequency: 16
Note: also known as HRPT1; associated with mutations in gene HRPT2 which codes for parafibromin
Date of Entry: 2012/08/24
Revision Date: 2021/08/09

Hyperparathyroidism 1 MeSH Supplementary Concept Data 2024