WormMine

WS296

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:331
Child Term . Identifier  DOID:0111003 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0111003 Joubert syndrome 8 A Joubert syndrome that has_material_basis_in mutation in the ARL13B gene on chromosome 3q11.1-q11.2.

1 Parent Term

Identifier Name Description
DOID:331 central nervous system disease A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system.