Search Ontology:
Human Disease

autosomal recessive cerebellar ataxia

Term ID
DOID:0050950
Synonyms
Definition
A cerebellar ataxia that has_material_basis_in autosomal recessive inheritance. http://www.ncbi.nlm.nih.gov/books/NBK1138/
References
  • MIM:PS213200
  • ORDO:1172
Ontology
Human Disease   ( DOID:0050950 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models
Citations