Global Variome shared LOVD

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Phenotype #0000166545 Individual ID 00218099 Associated disease - Phenotype details Alport Syndrom X-linked recessive Diagnosis/Initial moderate hearing loss / hematuria Inheritance Familial, X-linked Diagnosis/Definite alport syndrome Age/Examination 17y (17 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Viviana Karina Dalamón Database submission license No license selected Created by Viviana Karina Dalamón Date created 2019-01-22 16:29:46 +01:00 (CET) Date last edited 2019-01-22 20:49:05 +01:00 (CET)

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