WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:331
Child Term . Identifier  DOID:0070387 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0070387 developmental and epileptic encephalopathy 101 A developmental and epileptic encephalopathy characterized by early infantile epileptic encephalopathy and severe global developmental delay that has_material_basis_in homozygous mutation in the GRIN1 gene on chromosome 9q34.

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.