Fibrosis of extraocular muscles, congenital, 2

MONDO:0011181

Any congenital fibrosis of extraocular muscles in which the cause of the disease is a mutation in the PHOX2A gene.

Also known as: PHOX2A congenital fibrosis of extraocular muscles, congenital fibrosis of extraocular muscles caused by mutation in PHOX2A, fibrosis of extraocular muscles, congenital, 2, fibrosis of extraocular muscles, congenital, type 2, CFEOM2, Feom2 locus, fibrosis of extraocular muscles, congenital, autosomal recessive

6 clinical trials for this condition and its sub-types, 0 tagged with Fibrosis of extraocular muscles, congenital, 2 itself.

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↑ Congenital nervous system disorder (287) ↑ Congenital fibrosis of extraocular muscles (1)

Including sub-types (6) Tagged with Fibrosis of extraocular muscles, congenital, 2 (0)

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