Phenotype #0000051167

Individual ID 00060065
Associated disease CTRCT5
Phenotype details lameller cataract (Marner type)
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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-05-15 17:40:41 +02:00 (CEST)
Date last edited N/A

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