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:0080267 Direct  false
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0080267 autosomal dominant nonsyndromic deafness 71 An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the DMXL2 gene on chromosome 15q21.

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.