Phenotype #0000126361

Individual ID 00153684
Associated disease ATS2
Phenotype details hearing loss (HP:0000365); ocular changes; GBM pathology thinning, thickening, splitting; hematuria (HP:0000790); proteinuria (HP:0000093)
Diagnosis/Initial Alport syndrome
Inheritance Familial, autosomal recessive
Diagnosis/Definite syndrome, Alport, autosomal recessive (ASAR)
Age/Examination 25y (25 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Judy Savige
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-02-19 09:42:17 +01:00 (CET)
Date last edited 2018-02-21 12:26:09 +01:00 (CET)

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