Phenotype #0000119378

Individual ID 00146731
Associated disease LGMD2
Phenotype details -
Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive
Diagnosis/Definite LGMD-2I
Inheritance Isolated (sporadic)
Age/Examination -
Age/Onset -
Phenotype/Onset -
Age/Diagnosis -
Protein -
Owner name Lab Müller-Reible
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2007-08-31 17:44:39 +02:00 (CEST)
Date last edited 2012-03-09 18:26:59 +01:00 (CET)

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