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spinocerebellar ataxia type 15/16 | RareConnect | RareConnect.io

/autosomal dominant cerebellar ataxia type I

/spinocerebellar ataxia type 15/16

spinocerebellar ataxia type 15/16

Rare Disease

MONDO:0011694

Also Known As

SCA15/16SCAR16spinocerebellar ataxia type 15spinocerebellar ataxia type 15/16spinocerebellar ataxia type 16SCA15SCA16 (formerly)spinocerebellar ataxia 15spinocerebellar ataxia 16spinocerebellar ataxia 16 (formerly)spinocerebellar ataxia 16, formerly

Definition

Spinocerebellar ataxia type 15/16 (SCA15/16) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by cerebellar ataxia, tremor and cognitive impairment.

Patient-Friendly Information

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:606658 ↗

Orphanet

Orphanet:98769 ↗Orphanet:98770 ↗

GARD

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