Phenotype #0000305077

Individual ID 00413096
Associated disease MYOP
Phenotype details -
Diagnosis/Initial LGMD
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMDR5
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein IHC no SGCG (other SGCs present)
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 2022-07-11 16:33:01 +02:00 (CEST)
Date last edited 2022-07-11 16:45:05 +02:00 (CEST)

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