Phenotype #0000129966

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00155756
Associated disease	AHC1
Phenotype details	Abnormal eye movement, dystonia, automatic dysfunction, development delay.
Diagnosis/Initial	AHC
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	AHC
Age/Examination	00y08m (8 months)
Age/Diagnosis	00y08m
Age/Onset	00y06m
Phenotype/Onset	Abnormal eye movement
Protein	-
Owner name	Xiaoxu Yang
Database submission license	No license selected
Created by	Xiaoxu Yang
Date created	2018-06-24 18:45:02 +02:00 (CEST)
Date last edited	2018-06-26 09:05:36 +02:00 (CEST)

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