Ectopia lentis 1, isolated, autosomal dominant
MONDO:0007514Any isolated ectopia lentis in which the cause of the disease is a mutation in the FBN1 gene.
Also known as: ECTOL1, FBN1 isolated ectopia lentis, ectopia lentis 1, isolated, autosomal dominant, ectopia lentis, familial, isolated ectopia lentis caused by mutation in FBN1, autosomal dominant isolated ectopia lentis 1
1 clinical trial for this condition and its sub-types, 0 tagged with Ectopia lentis 1, isolated, autosomal dominant itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.