Disease #07261 (SCAR33 (ataxia, spinocerebellar, autosomal recessive, type 33), OMIM:620208)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	SCAR33
Name	ataxia, spinocerebellar, autosomal recessive, type 33
OMIM ID	620208
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RNU12
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-05-25 18:03:39 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.