Global Variome shared LOVD

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Phenotype #0000311320 Individual ID 00420085 Associated disease WRN Phenotype details see paper; ...; cataracts; skin anomalies; facial features; no short stature; greying or loss of hair; no diabetes mellitus; hypogonadism; osteoporosis; no osteosclerosis; no soft tissue calcification; no atherosclerosis; no neoplasms; voice change; no flat fee Diagnosis/Initial Werner syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite WRN Age/Examination 42y (42 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 08:50:16 +01:00 (CET) Date last edited 2022-10-31 08:57:49 +01:00 (CET)

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