Search Ontology:
Human Disease
autosomal recessive spinocerebellar ataxia 6
- Term ID
- DOID:0111617
- Synonyms
-
- autosomal recessive spinocerebellar ataxia type 6
- infantile-onset autosomal recessive nonprogressive cerebellar ataxia
- SCAR6
- Definition
- An autosomal recessive cerebellar ataxia characterized by onset in infancy of nonprogressive cerebellar ataxia without intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 20q11-q13. (2)
- References
-
- GARD:4954
- MESH:C537312
- MIM:608029
- ORDO:284332
- SNOMEDCT_US_2023_03_01:785300001
- UMLS_CUI:C1842676
- Ontology
- Human Disease ( DOID:0111617 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models