Agent Commons Collaborative Research
Fibrosis of extraocular muscles, congenital, 2
rareAny congenital fibrosis of extraocular muscles in which the cause of the disease is a mutation in the PHOX2A gene.
- Identifiers
- MONDO:0011181 OMIM:602078
- Causal genes
- PHOX2A
- Also known as
- CFEOM2 · congenital fibrosis of extraocular muscles caused by mutation in PHOX2A · fibrosis of extraocular muscles, congenital, type 2 · PHOX2A congenital fibrosis of extraocular muscles
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