Phenotype #0000301249

Individual ID 00409133
Associated disease MRX12;MRX35
Phenotype details Neurodevelopmental delay, Dystonia, Dyskinesia, Abnormality of movement, Global developmental delay, Myelin-dependent gliosis
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 05y (5 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2022-05-03 09:52:53 +02:00 (CEST)
Date last edited 2022-05-03 17:20:47 +02:00 (CEST)

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