MeSH Browser

MeSH Supplementary: Fibrosis Of Extraocular Muscles, Congenital, 2
Unique ID: C566587
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566587
Entry Term(s): CFEOM2; Fibrosis Of Extraocular Muscles, Congenital, Autosomal Recessive
Registry Number: 0
Heading Mapped to: *Blepharoptosis; *Fibrosis; *Ophthalmoplegia; *Eye Diseases, Hereditary
Frequency: 3
Note: mutation in ARIX
Date of Entry: 2012/11/05

Fibrosis Of Extraocular Muscles, Congenital, 2 MeSH Supplementary Concept Data 2024