Global Variome shared LOVD

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Phenotype #0000162042 Individual ID 00213588 Associated disease CMYO4A;CFTD Phenotype details - Diagnosis/Initial fiber-type disproportion, congenital Inheritance Isolated (sporadic) Diagnosis/Definite CFTD Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Tom Winder Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2012-09-28 22:39:01 +02:00 (CEST) Date last edited 2012-10-26 12:25:39 +02:00 (CEST)

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