Global Variome shared LOVD

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Phenotype #0000021125 Individual ID 00025005 Associated disease HRFTC Phenotype details see paper; congenital bilateral cataract, visual symptoms evident during infancy, glare and slowly progressive loss in visual acuity Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - 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 2014-11-30 20:21:56 +01:00 (CET) Date last edited N/A

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