Phenotype #0000127808

Individual ID 00155309
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 No license selected
Created by Johan den Dunnen