Global Variome shared LOVD

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Phenotype #0000207616 Individual ID 00269825 Associated disease HHT Phenotype details recurrent epistaxis, telangiectasia, visceral arteriovenous malformation, liver arteriovenous malformation, chronic HHT-related GI bleeding; family history Diagnosis/Initial telangiectasia Inheritance Familial, autosomal dominant Diagnosis/Definite HHT-2 Age/Examination 66y (66 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 2019-12-07 12:29:03 +01:00 (CET) Date last edited N/A

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