Disease #07085 (SPG89 (paraplegia, spastic, type 89, autosomal recessive), OMIM:620379)

Global Variome shared LOVD

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

Official abbreviation	SPG89
Name	paraplegia, spastic, type 89, autosomal recessive
OMIM ID	620379
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AMFR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-05-26 14:51:09 +02:00 (CEST)
Date last edited	N/A

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