Search Ontology:
Human Disease
Klippel-Feil syndrome 3
- Term ID
- DOID:0080591
- Synonyms
-
- 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
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations