MeSH Browser

MeSH Supplementary: Hypophosphatemic Rickets, Autosomal Dominant
Unique ID: C562791
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562791
Entry Term(s): Hypophosphatemia, Autosomal Dominant; Vitamin D-Resistant Rickets, Autosomal Dominant
Registry Number: 0
Heading Mapped to: *Rickets; *Familial Hypophosphatemic Rickets
Frequency: 6
Note: mutation in FGF23
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Hypophosphatemic Rickets, Autosomal Dominant MeSH Supplementary Concept Data 2024