Search Ontology:
Human Disease

Klippel-Feil syndrome 2

Term ID
DOID:0080590
Synonyms
Definition
A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MEOX1 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/23290072
References
Ontology
Human Disease   ( DOID:0080590 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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