Phenotype #0000119321

Individual ID 00146600
Associated disease LGMD2
Phenotype details mild with hCK, remained ambulant; CPK 6x
Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive
Diagnosis/Definite LGMD-2I
Inheritance Isolated (sporadic)
Age/Examination -
Age/Onset 14y
Phenotype/Onset shoulder girdle atrophy
Age/Diagnosis 29y
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 2007-08-31 17:40:57 +02:00 (CEST)
Date last edited 2012-03-09 19:02:28 +01:00 (CET)

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