Disease #03739 (SCAR13 (ataxia, spinocerebellar, autosomal recessive, type 13 (SCAR-13)), OMIM:614831)

Global Variome shared LOVD

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Official abbreviation	SCAR13
Name	ataxia, spinocerebellar, autosomal recessive, type 13 (SCAR-13)
OMIM ID	614831
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GRM1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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