Global Variome shared LOVD

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Phenotype #0000128931 Individual ID 00163811 Associated disease CPDX2 Phenotype details severe fetal form Diagnosis/Initial - Inheritance Familial Diagnosis/Definite CPDX-2 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Fabienne Dufernez Database submission license No license selected Created by Fabienne Dufernez Date created 2018-04-12 17:32:58 +02:00 (CEST) Date last edited N/A

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