Phenotype #0000078602

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00072203
Associated disease	DYT11
Phenotype details	see paper; ..., delay in motor development (HP:0001270), dystonia (HP:0001332), myoclonus (HP:0001336)
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	06y (6 years)
Age/Diagnosis	-
Age/Onset	02y08m
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2017-02-18 22:04:36 +01:00 (CET)
Date last edited	N/A

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