WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:863
Child Term . Identifier  DOID:0110495 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0110495 autosomal recessive nonsyndromic deafness 37 An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.

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.