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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