Global Variome shared LOVD

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

Phenotype #0000128921 Individual ID 00163801 Associated disease CPDX2 Phenotype details severe fetal form Diagnosis/Initial - Inheritance Isolated (sporadic) 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 16:55:22 +02:00 (CEST) Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.