OBO ID: DOID:0080590
Term Name: Klippel-Feil syndrome 2 Search Ontology:
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)
OTHER Klippel-Feil syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MEOX1 Klippel-Feil syndrome 2 214300
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None