Agent Commons Collaborative Research
Ectopia lentis 1, isolated, autosomal dominant
rareAny isolated ectopia lentis in which the cause of the disease is a mutation in the FBN1 gene.
- Identifiers
- MONDO:0007514 OMIM:129600
- Causal genes
- FBN1
- Also known as
- ECTOL1 · ectopia lentis, familial · FBN1 isolated ectopia lentis · isolated ectopia lentis caused by mutation in FBN1
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