Phenotype #0000129984

Individual ID 00163018
Associated disease AHC1
Phenotype details Abnormal eye movement, quadrplegia, epilepsy, and slight developmental delay.
Diagnosis/Initial AHC
Inheritance Familial, autosomal dominant
Diagnosis/Definite AHC
Age/Examination 01y (1 year)
Age/Diagnosis 01y
Age/Onset 00y01m
Phenotype/Onset Abnormal eye movement
Protein -
Owner name Xiaoxu Yang
Database submission license No license selected
Created by Xiaoxu Yang

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