Global Variome shared LOVD

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Phenotype #0000302464 Individual ID 00410360 Associated disease COXPD Phenotype details see paper; ..., hypertrophic cardiomyopathy, hyperlactatemia Diagnosis/Initial hypertrophic cardiomyopathy, hyperlactatemia Inheritance Familial, autosomal recessive Diagnosis/Definite COXPD23 Age/Examination 05y (5 years) 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 2022-05-25 09:59:49 +02:00 (CEST) Date last edited 2022-05-25 10:20:14 +02:00 (CEST)

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