Global Variome shared LOVD

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Phenotype #0000159196 Individual ID 00210631 Associated disease CGL Diagnosis/Initial congenital lipodystrophy, muscular dystrophy Diagnosis/Definite CGL-4 Phenotype details no acanthosis nigricans, fatty liver, no muscle weakness, myalgia, muscle stiffness, transient IgA deficiency, recurrent pneumonia; CPK 542-2253; no intellectual disability Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2009-11-07 16:58:46 +01:00 (CET) Date last edited 2013-02-01 19:44:12 +01:00 (CET)

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