Disease #00213 (SPG-10 (paraplegia, spastic, autosomal dominant, type 10 (SPG-10)), OMIM:604187)

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Official abbreviation	SPG-10
Name	paraplegia, spastic, autosomal dominant, type 10 (SPG-10)
OMIM ID	604187
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KIF5A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-02 11:35:03 +02:00 (CEST)
Date last edited	N/A