Phenotype #0000130102

Individual ID 00164006
Associated disease AHC
Diagnosis/Initial AHC
Diagnosis/Definite AHC
Phenotype details Hemiplegia first onset at 1m, quadriplegia, dystonia, epileptic seizure, dysphagia, dysarthria, ataxia, developmental delay, language delay
Inheritance Familial, autosomal dominant
Age/Examination 17y (17 years)
Age/Diagnosis 17y
Age/Onset 00y01m
Phenotype/Onset Hemiplegia
Protein -
Owner name Xiaoxu Yang
Database submission license No license selected
Created by Xiaoxu Yang
Date created 2018-07-02 01:38:59 +02:00 (CEST)
Date last edited 2018-07-02 14:03:59 +02:00 (CEST)

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