Phenotype #0000331182

Individual ID 00441771
Associated disease MECD
Phenotype details see paper; ...
Diagnosis/Initial Meesmann's corneal dystrophy
Inheritance Familial, autosomal dominant
Diagnosis/Definite MECD2
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 2010-03-16 16:56:37 +01:00 (CET)
Date last edited N/A

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