Global Variome shared LOVD

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Phenotype #0000311322 Individual ID 00420087 Associated disease WRN Phenotype details see paper; ..., cataracts; skin anomalies; facial features; short stature; greying or loss of hair; diabetes mellitus; hypogonadism; osteoporosis; osteosclerosis; soft tissue calcification; atherosclerosis; neoplasms; voice change; flat feet Diagnosis/Initial Werner syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite WRN Age/Examination 45y (45 years) Age/Diagnosis - Age/Onset - 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 2022-10-31 09:13:52 +01:00 (CET) Date last edited N/A

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