Term Name: autosomal dominant cerebellar ataxia
Synonyms: spinocerebellar ataxia
Definition: A cerebellar ataxia that has_material_basis_in autosomal dominant inheritance.
Ontology: Human Disease [DOID:1441]   ( DOID:1441 )

Relationships
is a type of: autosomal dominant disease cerebellar ataxia
has subtype: autosomal dominant cerebellar ataxia, deafness and narcolepsy cerebellar ataxia type 9 cerebellar ataxia type 41 cerebellar ataxia type 42 cerebellar ataxia type 43 cerebellar ataxia type 47 cerebellar ataxia type 48 dentatorubral-pallidoluysian atrophy GRID2-related spinocerebellar ataxia hypomyelinating leukoencephalopathy Machado-Joseph disease nonprogressive cerebellar ataxia with mental retardation spinocerebellar ataxia 44 spinocerebellar ataxia 45 spinocerebellar ataxia 46 spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spinocerebellar ataxia type 4 spinocerebellar ataxia type 5 spinocerebellar ataxia type 6 spinocerebellar ataxia type 7 spinocerebellar ataxia type 8 spinocerebellar ataxia type 10 spinocerebellar ataxia type 11 spinocerebellar ataxia type 12 spinocerebellar ataxia type 13 spinocerebellar ataxia type 14 spinocerebellar ataxia type 15 spinocerebellar ataxia type 17 spinocerebellar ataxia type 18 spinocerebellar ataxia type 19/22 spinocerebellar ataxia type 20 spinocerebellar ataxia type 21 spinocerebellar ataxia type 23 spinocerebellar ataxia type 25 spinocerebellar ataxia type 26 spinocerebellar ataxia type 27 spinocerebellar ataxia type 28 spinocerebellar ataxia type 29 spinocerebellar ataxia type 30 spinocerebellar ataxia type 31 spinocerebellar ataxia type 34 spinocerebellar ataxia type 35 spinocerebellar ataxia type 36 spinocerebellar ataxia type 37 spinocerebellar ataxia type 38 spinocerebellar ataxia type 40