Phenotype #0000105517

Individual ID 00132747
Associated disease NICCD
Phenotype details Hyperammonemia, hypercitrullinemia, galactosemia, cholestasis, hypoproteinemia
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 00y09m
Age/Onset <00y01m
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 2017-11-03 17:53:33 +01:00 (CET)
Date last edited N/A

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