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DO Term : Klippel-Feil syndrome 2 [DOID:0080590] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MEOX1 gene on chromosome 17q21.

synonyms:
214300,
OMIM:214300

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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