OBO ID: DOID:0111614 |
Term Name: | autosomal recessive spinocerebellar ataxia 22 | Search Ontology: | |
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Definition: | An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2. https://www.ncbi.nlm.nih.gov/pubmed/26157035 | ||
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Ontology: | Human Disease ( DOID:0111614 ) |
OTHER autosomal recessive spinocerebellar ataxia 22 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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VWA3B | ?Spinocerebellar ataxia, autosomal recessive 22 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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