Phenotype #0000130095

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00163999
Associated disease	AHC
Diagnosis/Initial	AHC
Diagnosis/Definite	AHC
Phenotype details	Abnormal eye movement, dystonia, automatic dysfunction, dysphagia, slight development delay
Inheritance	Familial, autosomal dominant
Age/Examination	02y (2 years)
Age/Diagnosis	02y
Age/Onset	00y03m
Phenotype/Onset	Abnormal eye movement
Protein	-
Owner name	Xiaoxu Yang
Database submission license	No license selected
Created by	Xiaoxu Yang
Date created	2018-07-02 00:41:46 +02:00 (CEST)
Date last edited	2018-07-02 14:00:17 +02:00 (CEST)

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