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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