Disease #07288 (SCAR31 (ataxia, spinocerebellar, autosomal recessive, type 31), OMIM:619422)

Global Variome shared LOVD

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Official abbreviation	SCAR31
Name	ataxia, spinocerebellar, autosomal recessive, type 31
OMIM ID	619422
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ATG7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-10-30 11:21:43 +01:00 (CET)
Date last edited	N/A

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