Phenotype #0000129979

Individual ID 00163013
Associated disease AHC1
Phenotype details Dystonia, Abnormal eye movement, quadriplegia, and slight developmental delay
Diagnosis/Initial AHC
Inheritance Familial, autosomal dominant
Diagnosis/Definite AHC
Age/Examination 01y (1 year)
Age/Diagnosis 01y
Age/Onset 00y02m
Phenotype/Onset dystonia
Protein -
Owner name Xiaoxu Yang
Database submission license No license selected
Created by Xiaoxu Yang

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