Phenotype #0000128919

Individual ID 00163799
Associated disease CPDX2
Phenotype details severe fetal form
Diagnosis/Initial -
Inheritance Familial, X-linked
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 16:40:28 +02:00 (CEST)
Date last edited 2018-04-12 16:48:06 +02:00 (CEST)

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