Phenotype #0000130103

Individual ID 00164007
Associated disease AHC
Diagnosis/Initial AHC
Diagnosis/Definite AHC
Phenotype details Hemiplegia first onset at 7m, 2-3 times/m, dystonia, epileptic seizure, automatic dysfunction, dysphagia, respiritary disturbance, slight developmental delay, language delay
Inheritance Familial, autosomal dominant
Age/Examination 02y (2 years)
Age/Diagnosis 02y
Age/Onset 00y07m
Phenotype/Onset Dystonia and hemiplegia
Protein -
Owner name Xiaoxu Yang
Database submission license No license selected
Created by Xiaoxu Yang
Date created 2018-07-02 01:45:41 +02:00 (CEST)
Date last edited 2018-07-02 14:04:51 +02:00 (CEST)

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