Hypophosphatemic Rickets, Autosomal Dominant [Supplementary Concept]

mutation in FGF23

Date introduced: November 5, 2012

MeSH Unique ID: C562791

Heading Mapped to:

• Rickets
• Familial Hypophosphatemic Rickets

Entry Terms:

• Hypophosphatemia, Autosomal Dominant
• Vitamin D-Resistant Rickets, Autosomal Dominant