Phenotype #0000044452

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00057801
Associated disease	SPG3A
Phenotype details	childhood-onset spastic gait, similarly affected child, no previous family history of hereditary spastic paraplegia
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2012-11-05 13:33:58 +01:00 (CET)
Date last edited	2017-01-03 20:51:54 +01:00 (CET)

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