MeSH Browser

MeSH Supplementary: Hypoparathyroidism, X-Linked
Unique ID: C562782
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562782
Registry Numbers: 0
Heading Mapped to: *Hypoparathyroidism; Parathyroid Glands / abnormalities; *Genetic Diseases, X-Linked
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Hypoparathyroidism, X-Linked MeSH Supplementary Concept Data 2025