Phenotype #0000333386

Individual ID 00444132
Associated disease CTRCT
Phenotype details see paper; ...
Diagnosis/Initial bilateral cataracts
Inheritance Familial, autosomal dominant
Diagnosis/Definite CTRCT2
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-12-18 17:46:20 +01:00 (CET)
Date last edited N/A

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