Phenotype #0000129967

Individual ID 00155757
Associated disease AHC1
Phenotype details Abnormal eye movement, quadriplegia, dystonia, ataxia, epilepsy, and developmental delay
Diagnosis/Initial AHC
Inheritance Familial, autosomal dominant
Diagnosis/Definite AHC
Age/Examination 03y (3 years)
Age/Diagnosis 03y
Age/Onset 01y
Phenotype/Onset Abnormal eye movement
Protein -
Owner name Xiaoxu Yang
Database submission license No license selected
Created by Xiaoxu Yang

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