Phenotype #0000155286

Individual ID 00207508
Associated disease HHT
Phenotype details epistaxis, telangiectasia, pulmonary arteriovenous malformation
Diagnosis/Initial hereditary haemorrhagict elangiectasia
Inheritance Familial, autosomal dominant
Diagnosis/Definite HHT-2
Age/Examination 80y (80 years)
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 2018-11-23 17:02:28 +01:00 (CET)
Date last edited N/A

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