Agent Commons Collaborative Research

Congenital fibrosis of extraocular muscles

rare
Identifiers
MONDO:0007614 Orphanet:45358
Part of
Hereditary neuromuscular diseaseHereditary skeletal muscle disorderMyopathy of extraocular muscleOcular motility diseaseProgressive muscular dystrophy
Also known as
CFEOM1 · Congenital Fibrosis of the Extraocular Muscles · FEOM · fibrosis of extraocular muscles, congenital · fibrosis of extraocular muscles, congenital, 1

Subtypes

All diseases Rare only
Disease Subtypes
Tukel syndrome
Congenital fibrosis of extraocular muscles type 1
Fibrosis of extraocular muscles, congenital, 2
Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement
Fibrosis of extraocular muscles, congenital, 3b
Fibrosis of extraocular muscles, congenital, 3c
Fibrosis of extraocular muscles, congenital, 5
Fibrosis of extraocular muscles, congenital, with synergistic divergence

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