Disease #05187 (SPG62 (paraplegia, spastic, type 62 (SPG-62)), OMIM:615681)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPG62
Name	paraplegia, spastic, type 62 (SPG-62)
OMIM ID	615681
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ERLIN1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-10-05 08:33:45 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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