Global Variome shared LOVD

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Phenotype #0000165212 Individual ID 00216760 Associated disease WRN Phenotype details familial partial lipodystrophy of the Dunnigan type (FPLD2), progeroid features; see paper Diagnosis/Initial Werner syndrome, atypical Inheritance Isolated (sporadic) Diagnosis/Definite HGPS Age/Examination - Age/Diagnosis - Age/Onset 12y Phenotype/Onset short stature Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2014-03-21 15:55:05 +01:00 (CET) Date last edited N/A

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