WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:0050950
Child Term . Identifier  DOID:0111616 Direct  true
Redundant  false

1 Child Term

Identifier Name Description
DOID:0111616 autosomal recessive spinocerebellar ataxia 27 An autosomal recessive cerebellar ataxia characterized by adult onset of progressive gait difficulties and other cerebellar signs that has_material_basis_in homozygous or compound heterozygous mutation in the GDAP2 gene on chromosome 1p12.

1 Parent Term

Identifier Name Description
DOID:0050950 autosomal recessive cerebellar ataxia A cerebellar ataxia that has_material_basis_in autosomal recessive inheritance.