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
Ontology
Human Disease   ( DOID:0050950 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models