Search Ontology:

Human Disease

X-linked cerebellar ataxia

Term ID

DOID:0111828

Synonyms

Definition

A hereditary ataxia characterized by X-linked inheritance. https://www.ncbi.nlm.nih.gov/pubmed/10807077

References

ORDO:247765

Ontology

Human Disease ( DOID:0111828 )

Relationships

is a type of: X-linked hereditary ataxia

X-linked hereditary ataxia Show first 5 Terms
has subtype: X-linked spinocerebellar ataxia 1 X-linked spinocerebellar ataxia 2 X-linked spinocerebellar ataxia 3 X-linked spinocerebellar ataxia 4 X-linked spinocerebellar ataxia 5

X-linked spinocerebellar ataxia 1 X-linked spinocerebellar ataxia 2 X-linked spinocerebellar ataxia 3 X-linked spinocerebellar ataxia 4 X-linked spinocerebellar ataxia 5 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models