Disease #05429 (SCAR21 (ataxia, spinocerebellar, autosomal recrecessive, type 21 (SCAR-21)), OMIM:616719)

Official abbreviation	SCAR21
Name	ataxia, spinocerebellar, autosomal recrecessive, type 21 (SCAR-21)
OMIM ID	616719
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCYL1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2018-05-20 10:46:55 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD