Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000127748 Individual ID 00155198 Associated disease CPDX2 Phenotype details severe foetal form Diagnosis/Initial chondrodysplasia punctata Inheritance Isolated (sporadic) Diagnosis/Definite CDPX-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 2018-03-13 16:18:43 +01:00 (CET) Date last edited 2018-03-15 15:41:26 +01:00 (CET)

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