Phenotype #0000238115

Individual ID 00313792
Associated disease LGMD
Phenotype details muscle weakness lower extremity, involvement proximal muscles upper limb shoulder girdle; serum CK 3768 U/L; no cardiac involvement
Diagnosis/Initial limb-girdle muscular dystrophy
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMD2L
Age/Examination -
Age/Diagnosis -
Age/Onset 33y
Phenotype/Onset -
Protein -
Owner name Ieke Ginjaar
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-10-06 10:37:52 +02:00 (CEST)
Date last edited N/A

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