Global Variome shared LOVD

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Phenotype #0000179993 Individual ID 00239779 Associated disease AHC Phenotype details see paper; ..., Duchenne muscular dystrophy, glycerol kinase deficiency; 6y-central precocious puberty Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite DMD;AHC;GKD Age/Examination 16y (16 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2019-06-09 10:27:56 +02:00 (CEST) Date last edited N/A

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