Global Variome shared LOVD

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Phenotype #0000164925 Individual ID 00216473 Associated disease HGPS Phenotype details combined phenotype of progeria and myopathy Diagnosis/Initial progeria, syndrome, Hutchinson-Gilford (HGPS);MD Inheritance Isolated (sporadic) Diagnosis/Definite HGPS Age/Examination - Age/Diagnosis - Age/Onset 0y Phenotype/Onset - Protein - Owner name Janbernd Kirschner 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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