Phenotype #0000366510

Individual ID 00483745
Associated disease LGMDR2;LGMD2B
Phenotype details see paper; ..., age onset 21.7±7y (14y-39y), age diagnosis 49±16y; disease duration 28.5±16y; 21/23 had affected members
Diagnosis/Initial muscle weakness
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMDR2
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 2026-08-11 14:58:59 +02:00 (CEST)
Date last edited N/A

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