Global Variome shared LOVD

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Phenotype #0000334180 Individual ID 00444930 Associated disease CTRCT Phenotype details see paper; ..., nuclear cataract, full ocular movements, clear conjunctiva, normal anterior chamber Diagnosis/Initial cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT2 Age/Examination 04y (4 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-12-28 19:43:58 +01:00 (CET) Date last edited N/A

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