Global Variome shared LOVD

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Phenotype #0000052816 Individual ID 00073136 Associated disease CCTRCT Phenotype details bilateral lamellar cataract (HP:0007971) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis 12y Age/Onset - Phenotype/Onset - Protein - Owner name Jamie Zeegers Database submission license No license selected Created by Jamie Zeegers Date created 2016-06-08 11:55:31 +02:00 (CEST) Date last edited 2017-07-11 21:53:27 +02:00 (CEST)

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