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Aniridia

MONDO:0019172

Aniridia is a congenital ocular malformation characterized by the complete or partial absence of the iris. It can be isolated or part of a syndrome (isolated and syndromic aniridia).

Also known as: aplasia of iris

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

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Sub-types

Aniridia 1 (0) Aniridia 2 (0) Aniridia 3 (0) Isolated aniridia (0) Zazam Sheriff Phillips syndrome (0)

Broader categories

Disease (618) Eye disorder (97) Human disease (14) Disorder of orbital region (3) Disorder of visual system (1) Uveal disorder (1) Disease by body system or component (0) Disease by developmental or physiological process (0) Disorder of development or morphogenesis (0) Iris disorder (0)
Trials to join now! 12 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2 Terminated 1
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  • Scientists hunt for biomarkers to unlock rare eye disease treatments

    Knowledge-focused Not yet recruiting

    This study aims to find biological markers (biomarkers) in blood, tears, and eye cells from 110 adults with seven rare eye diseases. Researchers will compare these markers between patients and healthy controls to see if they differ and if they relate to disease symptoms. The goal…

    Phase: NA • Sponsor: Institut National de la Santé Et de la Recherche Médicale, France • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:02 UTC

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