Phenotype #0000128135

Individual ID 00155755
Associated disease AHC1
Phenotype details The patient had the first symptom on set at the age of 5.5m, his first hemiplegia starts at the age of 8m, the duration rangers from 1 to 2 days, he has abnormal eye movemetn and dystonia.
Diagnosis/Initial AHC-1
Inheritance Familial, autosomal dominant
Diagnosis/Definite AHC-1
Age/Examination 04y (4 years)
Age/Diagnosis 04y
Age/Onset 00y05m
Phenotype/Onset -
Protein -
Owner name Xiaoxu Yang
Database submission license No license selected
Created by Xiaoxu Yang