Fibrosis of Extraocular Muscles, Congenital, 3B [Supplementary Concept]
PROM mutation in KIF21A
Date introduced: November 5, 2012
MeSH Unique ID: C567739
Heading Mapped to:
Entry Terms:
- CFEOM3B
- Fibrosis Of Extraocular Muscles, Congenital, 1
- Blepharoptosis with Absent Eye Movements
- CFEOM1
- Ophthalmoplegia, Congenital
- FEOM1