Phenotype #0000297163

Individual ID 00404579
Associated disease argininemia
Phenotype details see paper; ..., learning difficulties, spastic diplegia, seizures, recurrent hyperammonemic episodes
Diagnosis/Initial argininemia
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 08y
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 2022-03-04 16:50:58 +01:00 (CET)
Date last edited 2022-03-04 17:01:48 +01:00 (CET)

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