Phenotype #0000105520

Individual ID 00132750
Associated disease CTLN2
Phenotype details hyperammonemia, hypercitrullinemia
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 28y
Phenotype/Onset loss of consciousness, vomiting, seizures
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 18:18:11 +01:00 (CET)
Date last edited N/A

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