WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:863
Child Term . Identifier  DOID:0111002 Direct  false
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0111002 Joubert syndrome 7 A Joubert syndrome that has_material_basis_in mutation in the RPGRIP1L gene on chromosome 16q12.2.

1 Parent Term

Identifier Name Description
DOID:863 nervous system disease A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.