Phenotype #0000356198

Individual ID 00471361
Associated disease DYT
Diagnosis/Initial dystonia
Diagnosis/Definite SPG4
Phenotype details combined dystonia, coexisting non-movement disorder-related neurological symptoms; onset infancy (0-2y); focal dystonia; dystonic cerebral palsy
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
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 2025-12-19 18:53:19 +01:00 (CET)
Date last edited N/A

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