WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:0080015
Child Term . Identifier  DOID:0080592 Direct  false
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0080592 Klippel-Feil syndrome 4 A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MYO18B gene on chromosome 22q12.

1 Parent Term

Identifier Name Description
DOID:0080015 physical disorder A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment.