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Early-onset non-syndromic cataract
Early-onset non-syndromic cataract is a rare, genetic, non-syndromic developmental defect of the eye, with high clinical and genetic heterogeneity, most frequently characterized by bilateral, symmetrical, non-progressive cataracts which present at birth or in early-childhood. Additional ocular manifestations (e.g. anterior segment dysgenesis, colobomas, nystagmus, microcornea, microphthalmia, myopia) may be associated, however other organs/systems are usually not affected.
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Early-onset partial cataract 0 trials · 1 incl. sub-types Sub-types →
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Cataract 10 multiple types 0 trials
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Cataract 11 multiple types 0 trials
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Cataract 13 with adult I phenotype 0 trials
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Cataract 14 multiple types 0 trials
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Cataract 15 multiple types 0 trials
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Cataract 17 multiple types 0 trials
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Cataract 19 multiple types 0 trials
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Cataract 20 multiple types 0 trials
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Cataract 21 multiple types 0 trials
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Cataract 22 multiple types 0 trials
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Cataract 23 0 trials
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Cataract 26 multiple types 0 trials
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Cataract 31 multiple types 0 trials
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Cataract 32 multiple types 0 trials
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Cataract 33 0 trials
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Cataract 38 0 trials
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Cataract 39 multiple types 0 trials
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Cataract 40 0 trials
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Cataract 42 0 trials
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Cataract 43 0 trials
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Cataract 44 0 trials
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Cataract 45 0 trials
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Cataract 46 juvenile-onset 0 trials
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Cataract 5 multiple types 0 trials
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Cataract 6 multiple types 0 trials
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Cataract 8 multiple types 0 trials
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Pulverulent cataract 0 trials
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Total early-onset cataract 0 trials