Phenotype #0000127807

Individual ID 00155308
Associated disease FECD
Phenotype details see paper; …
Diagnosis/Initial dystrophy, corneal, Fuchs endothelial
Inheritance Familial, autosomal dominant
Diagnosis/Definite FECD-3
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 2018-03-23 10:15:07 +01:00 (CET)
Date last edited N/A

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