Phenotype #0000337701

Individual ID 00448525
Associated disease DYT11
Phenotype details HP:0001332 Dystonia, HP:0002333 Motor deterioration, HP:0001336 Myoclonus, HP:0001337 Tremor.
Diagnosis/Initial 56
Inheritance Familial, autosomal dominant
Diagnosis/Definite Dystonia-11, myoclonic (AD, #159900)
Age/Examination 32
Age/Diagnosis 56y
Age/Onset 21y
Phenotype/Onset -
Protein -
Owner name Maria Elena García Paya
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maria Elena García Paya
Date created 2024-03-26 12:12:38 +01:00 (CET)
Date last edited 2024-04-08 14:01:53 +02:00 (CEST)

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