Phenotype #0000125594

Individual ID 00152665
Associated disease ATS
Phenotype details microscopic hematuria, leiomyomatosis of the eosophagus, billateral cataract
Diagnosis/Initial Alport syndrome with leiomyomatosis
Inheritance Familial, X-linked dominant
Diagnosis/Definite Alport syndrome with leiomyomatosis
Age/Examination 01y (1 year)
Age/Diagnosis 01y
Age/Onset <00y06m
Phenotype/Onset <6m
Protein -
Owner name Pavlina Plevova
Database submission license No license selected
Created by Pavlina Plevova
Date created 2018-02-05 21:17:58 +01:00 (CET)
Date last edited 2018-02-16 14:23:11 +01:00 (CET)

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