WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:0050557
Child Term . Identifier  DOID:0112375 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0112375 muscular dystrophy-dystroglycanopathy type B A muscular dystrophy-dystroglycanopathy characterized by early onset of muscle weakness, intellectual disability in most cases, and variable presence of mild brain anomalies.

1 Parent Term

Identifier Name Description
DOID:0050557 congenital muscular dystrophy A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted.