Congenital fibrosis of extraocular muscles type 1

MONDO:0021083

Any congenital fibrosis of extraocular muscles in which the cause of the disease is a mutation in the KIF21A gene.

Also known as: CFEOM1, KIF21A congenital fibrosis of extraocular muscles, congenital fibrosis of extraocular muscles caused by mutation in KIF21A, fibrosis of extraocular muscles, congenital, 1, Feom1 locus, blepharoptosis with absent eye movements, fibrosis of extraocular muscles, congenital, 3B, ophthalmoplegia, congenital

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