Global Variome shared LOVD

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Phenotype #0000052011 Individual ID 00072342 Associated disease CCTRCT Phenotype details impaired visual acuity (HP:0030532), lens opacity (HP:0000518), opacity in the central nucleus region of both lenses (HP:0000518), Y-sutures were also involved with prominent opacity (HP:?), no systemic disease (-HP:?), no other ocular disease (-HP:?) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jamie Zeegers Database submission license No license selected Created by Jamie Zeegers Date created 2016-06-06 10:39:30 +02:00 (CEST) Date last edited 2017-07-11 20:56:24 +02:00 (CEST)

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