Search Ontology:
Human Disease
autosomal recessive spinocerebellar ataxia 34
- Term ID
- DOID:0070558
- Synonyms
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- CAMRQ syndrome 3
- CAMRQ3
- cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3
- Definition
- An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CA8 gene on chromosome 8q12.1. (3)
- References
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- MESH:C567690
- MIM:613227
- UMLS_CUI:C2750509
- Ontology
- Human Disease ( DOID:0070558 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models