Cutis Gyrata Syndrome of Beare And Stevenson [Supplementary Concept]
mutation in FGFR2
Date introduced: November 5, 2012
MeSH Unique ID: C565129
Heading Mapped to:
Entry Terms:
- Beare-Stevenson Cutis Gyrata Syndrome
- Cutis Gyrata Syndrome of Beare-Stevenson