Disease

autosomal recessive spinocerebellar ataxia 17

Name: autosomal recessive spinocerebellar ataxia 17
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0080064 autosomal recessive spinocerebellar ataxia 17 An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24. SCAR17

Definition

An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24.

Synonyms

SCAR17

Cross References

MIM:616127

Parent Terms

autosomal recessive cerebellar ataxia

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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