Global Variome shared LOVD

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

Phenotype #0000164744 Individual ID 00216292 Associated disease WRN Phenotype details atypical mandibuloacral dysplasia and progeroid features Diagnosis/Initial Werner syndrome Inheritance Isolated (sporadic) Diagnosis/Definite HGPS Age/Examination - Age/Diagnosis - Age/Onset 5y Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2007-08-31 18:26:59 +02:00 (CEST) Date last edited 2012-03-09 19:17:22 +01:00 (CET)

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