Phenotype #0000232680

Individual ID 00306852
Associated disease Gilbert syndrome
Phenotype details Kernicterus, anemia, unconjugated hyperbilirubinemia
Diagnosis/Initial -
Inheritance Familial
Diagnosis/Definite -
Age/Examination 17y (17 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Nawel Trabelsi
Database submission license No license selected
Created by Nawel Trabelsi
Date created 2020-07-21 16:39:04 +02:00 (CEST)
Date last edited 2020-09-11 11:47:26 +02:00 (CEST)

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