WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:10426
Child Term . Identifier  DOID:0080589 Direct  true
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0080589 Klippel-Feil syndrome 1 A Klippel-Feil syndrome that has_material_basis_in heterozygous mutation in the GDF6 gene on chromosome 8q22.

1 Parent Term

Identifier Name Description
DOID:10426 Klippel-Feil syndrome A physical disorder that is characterized by abnormal segmentation of the vertebra during fetal development which results in fusion located in cervical vertebra.