Phenotype #0000127082

Individual ID 00111886
Associated disease myotonia
Phenotype details -
Diagnosis/Initial myotonia congenita
Inheritance Familial, autosomal recessive
Diagnosis/Definite Becker disease
Age/Examination -
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 2018-02-23 17:58:57 +01:00 (CET)
Date last edited 2018-02-24 09:08:40 +01:00 (CET)

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