Phenotype #0000128135

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00155755
Associated disease	AHC1
Phenotype details	The patient had the first symptom on set at the age of 5.5m, his first hemiplegia starts at the age of 8m, the duration rangers from 1 to 2 days, he has abnormal eye movemetn and dystonia.
Diagnosis/Initial	AHC-1
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	AHC-1
Age/Examination	04y (4 years)
Age/Diagnosis	04y
Age/Onset	00y05m
Phenotype/Onset	-
Protein	-
Owner name	Xiaoxu Yang
Database submission license	No license selected
Created by	Xiaoxu Yang
Date created	2018-03-31 11:35:40 +02:00 (CEST)
Date last edited	2018-04-03 21:01:33 +02:00 (CEST)

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