Disease #06068 (SPG9B (Spastic paraplegia 9B, autosomal recessive), OMIM:616586)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Johan den Dunnen

Official abbreviation	SPG9B
Name	Spastic paraplegia 9B, autosomal recessive
OMIM ID	616586
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALDH18A1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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