Phenotype #0000165211

Individual ID 00216759
Associated disease WRN
Phenotype details short stature, progeroid appearance, beaked nose, scleroderma-like skin, premature grayin,d alopecia, atrophic skin, dystrophic nails
Diagnosis/Initial Werner syndrome, atypical
Inheritance Isolated (sporadic)
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 2014-03-21 15:55:05 +01:00 (CET)
Date last edited N/A

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