OBO ID: DOID:0080590 |
Term Name: | Klippel-Feil syndrome 2 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0080590 ) |
OTHER Klippel-Feil syndrome 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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