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PAX6-related ocular dysgenesis

MONDO:0800183

Any eye disorder in which the cause of the disease is a mutation in the PAX6 gene.

2878 clinical trials for this condition and its sub-types, 0 tagged with PAX6-related ocular dysgenesis itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary neurological disease (5791) ↑ Hereditary renal cell carcinoma (7) ↑ Eye carcinoma (5) ↑ SMARCB1-deficient kidney medullary carcinoma (4)

Sub-types of PAX6-related ocular dysgenesis

Including sub-types (2878) Tagged with PAX6-related ocular dysgenesis (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.