WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:0080000
Child Term . Identifier  DOID:0110288 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0110288 autosomal recessive limb-girdle muscular dystrophy type 2W An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in compound heterozygous mutation in the LIM zinc finger domain containing 2 gene (LIMS2) on chromosome 2q14.

1 Parent Term

Identifier Name Description
DOID:0080000 muscular disease A musculoskeletal system disease that affects the muscles.