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Ectopia lentis 1, isolated, autosomal dominant

MONDO:0007514

Any 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

10 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Eye disorder (97) Human disease (14) Lens disorder (10) Disorder of orbital region (3) Isolated ectopia lentis (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Disease by body system or component (0)
Trials to join now! 7 Not yet finished but already full! 1 Completed 1 Terminated 1
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  • Free eye tests aim to catch vision loss early in harlem and washington heights

    Knowledge-focused Ongoing

    This study offers free vision screenings to underserved adults over 40 living in affordable housing in Harlem and Washington Heights. The goal is to find eye problems like glaucoma, cataracts, and diabetic retinopathy early and connect people with follow-up care. About 749 partic…

    Phase: NA • Sponsor: Columbia University • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:54 UTC

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