Search Ontology:
Human Disease
Klippel-Feil syndrome 3
- Term ID
- DOID:0080591
- Synonyms
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- Definition
- A Klippel-Feil syndrome that has_material_basis_in heterozygous mutation in the GDF3 gene on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/19864492
- References
- Ontology
- Human Disease ( DOID:0080591 )
- is a type of
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