Search Ontology:
Human Disease
Klippel-Feil syndrome 2
- Term ID
- DOID:0080590
- Synonyms
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- 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 )
- is a type of
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