Phenotype #0000340320

Individual ID 00451659
Associated disease CTLN1
Phenotype details Mild Intellectual disability, Seizures.
Diagnosis/Initial Citrullinemia
Inheritance Familial, autosomal recessive
Diagnosis/Definite Citrullinemia
Age/Examination -
Age/Diagnosis 07y
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Miriam Erandi Reyna-Fabián
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Miriam Erandi Reyna-Fabián
Date created 2024-06-21 22:11:38 +02:00 (CEST)
Date last edited 2024-06-28 10:11:15 +02:00 (CEST)

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