Phenotype #0000001862

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00003011
Associated disease	SPG10
Phenotype details	hereditary spastic paraplegia
Diagnosis/Initial	hereditary spastic paraplegia
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	47y
Phenotype/Onset	-
Protein	-
Owner name	Marcel Nelen
Database submission license
Created by	Julia Lopez
Date created	2013-10-02 11:35:03 +02:00 (CEST)
Date last edited	2022-11-17 09:36:50 +01:00 (CET)

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