Global Variome shared LOVD

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Phenotype #0000027417 Individual ID 00034019 Associated disease CTRCT Phenotype details see paper; ..., congenital, nuclear cataract Diagnosis/Initial cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT2 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Lu Cailing Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Lu Cailing Date created 2011-10-18 09:14:59 +02:00 (CEST) Date last edited 2023-12-27 20:46:51 +01:00 (CET)

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