MeSH Browser

MeSH Supplementary: Hyperparathyroidism 2
Unique ID: C563273
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563273
Entry Term(s): Familial Cystic Parathyroid Adenomatosis; Familial Primary Hyperparathyroidism with Multiple Ossifying Jaw Fibromas; Hereditary Hyperparathyroidism-Jaw Tumor Syndrome; Hpt-Jt; Hyperparathyroidism, Familial Primary, with Multiple Ossifying Jaw Fibromas; Hyperparathyroidism-Jaw Tumor Syndrome; Hyperparathyroidism-Jaw Tumor Syndrome, Hereditary
Registry Numbers: 0
Heading Mapped to: *Adenoma; *Fibroma; *Hyperparathyroidism; *Jaw Neoplasms
Frequency: 38
Date of Entry: 2012/11/05
Revision Date: 2014/08/08

Hyperparathyroidism 2 MeSH Supplementary Concept Data 2025