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Autosomal recessive nonsyndromic congenital nuclear cataract

MONDO:0021957

Also known as: congenital nuclear cataract, autosomal recessive

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

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Broader categories

Disease (618) Cataract (235) Hereditary disease (172) Eye disorder (97) Human disease (14) Lens disorder (10) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Early-onset non-syndromic cataract (1)
Trials to join now! 7 Not yet finished but already full! 1 Completed 1 Terminated 1
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