Phenotype #0000129976

Individual ID 00163010
Associated disease AHC1
Phenotype details dystonia, Abnormal eye movement, automatic dysfunction, dysphagia, dysarthria, and developmental delay.
Diagnosis/Initial AHC
Inheritance Familial, autosomal dominant
Diagnosis/Definite AHC
Age/Examination 03y (3 years)
Age/Diagnosis 03y
Age/Onset 00y01m
Phenotype/Onset dystonia
Protein -
Owner name Xiaoxu Yang
Database submission license No license selected
Created by Xiaoxu Yang

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