Phenotype #0000119649

Individual ID 00146586
Associated disease LGMD
Phenotype details proximal muscle weakness lower extremities, involvement proximal muscles upper limb/shoulder girdle in disease course, no cardiac involvement
Diagnosis/Initial dystrophy, muscular, limb-girdle
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMD2I
Age/Examination -
Age/Diagnosis -
Age/Onset 15y
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 2007-08-31 17:40:57 +02:00 (CEST)
Date last edited 2020-10-04 11:04:50 +02:00 (CEST)

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