Phenotype #0000238636

Individual ID 00314878
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details movement disorder; epilepsy; hypotonia; severe developmental delay
Inheritance Isolated (sporadic)
Age/Examination 07y (7 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
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 2020-10-20 15:09:17 +02:00 (CEST)
Date last edited 2023-10-19 15:33:21 +02:00 (CEST)

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