Disease #07168 (SPG87 (spastic paraplegia, type 87), OMIM:619966)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPG87
Name	spastic paraplegia, type 87
OMIM ID	619966
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMEM63C
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-06-19 11:12:45 +02:00 (CEST)
Date last edited	N/A

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