Phenotype #0000164905

Individual ID 00216453
Associated disease WRN
Phenotype details atypical WRN (19y), cleroderma-like skin, short stature, graying/thinning of hair, type 2 diabetes (18y)
Diagnosis/Initial Werner syndrome
Inheritance Unknown
Diagnosis/Definite HGPS
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2007-08-31 18:26:59 +02:00 (CEST)
Date last edited 2012-03-09 19:39:26 +01:00 (CET)

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