Phenotype #0000222765

Individual ID 00289132
Associated disease MYOP
Phenotype details LGMD
Diagnosis/Initial myopathy
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMD2L
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 2020-03-01 11:31:09 +01:00 (CET)
Date last edited N/A

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