MeSH Browser

MeSH Supplementary: Fibrosis of Extraocular Muscles, Congenital, 3B
Unique ID: C567739
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567739
Entry Term(s): Blepharoptosis with Absent Eye Movements; CFEOM1; CFEOM3B; FEOM1; Fibrosis Of Extraocular Muscles, Congenital, 1; Ophthalmoplegia, Congenital
Registry Numbers: 0
Heading Mapped to: *Fibrosis; *Eye Diseases, Hereditary; *Ocular Motility Disorders
Frequency: 19
Note: PROM mutation in KIF21A
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Concept UI: M0565314
Registry Numbers: 0
Terms: Fibrosis Of Extraocular Muscles, Congenital, 1 Preferred Term
Term UI T806002
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Blepharoptosis with Absent Eye Movements
Term UI T824556
Date06/22/2012
LexicalTag NON
ThesaurusID OMIM (2013); CFEOM1
Term UI T823635
Date06/14/2012
LexicalTag NON
ThesaurusID OMIM (2013); Ophthalmoplegia, Congenital
Term UI T806006
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); FEOM1
Term UI T824555
Date06/22/2012
LexicalTag NON
ThesaurusID OMIM (2013)

Fibrosis of Extraocular Muscles, Congenital, 3B MeSH Supplementary Concept Data 2025