Global Variome shared LOVD

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

Phenotype #0000232858 Individual ID 00307032 Associated disease ? Diagnosis/Initial - Diagnosis/Definite HPDL deficiency disorder Phenotype details - Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Wenjuan Qiu Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Wenjuan Qiu Date created 2020-07-28 10:47:19 +02:00 (CEST) Date last edited 2020-07-29 09:07:27 +02:00 (CEST)

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