Global Variome shared LOVD

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Phenotype #0000257385 Individual ID 00361992 Associated disease CPN1D Phenotype details Proband presenting with a CPN deficiency clinical phenotype, i.e. association of chronic urticaria and angioedema Diagnosis/Initial - Inheritance Familial Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Christian Drouet Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Christian Drouet Date created 2021-04-13 11:47:27 +02:00 (CEST) Date last edited N/A

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