Phenotype #0000129987

Individual ID 00163021
Associated disease AHC1
Phenotype details Epilepsy, Abnormal eye movement, Dystonia, automatic dysfunction, and slight developmental delay.
Diagnosis/Initial AHC
Inheritance Familial, autosomal dominant
Diagnosis/Definite AHC
Age/Examination 02y (2 years)
Age/Diagnosis 02y
Age/Onset 00y01m
Phenotype/Onset seizure
Protein -
Owner name Xiaoxu Yang
Database submission license No license selected
Created by Xiaoxu Yang

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