SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21; SCAR21

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Summary

Literature (0)

MIM:616719 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21; SCAR21

Xenbase Genes: scyl1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014744 - acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome

MONDO:0014744 - acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome

Disease Ontology (DO):

DOID:0111155 - autosomal recessive spinocerebellar ataxia 21

DOID:0111155 - autosomal recessive spinocerebellar ataxia 21