OBO ID: DOID:0080592
Term Name: Klippel-Feil syndrome 4 Search Ontology:
Synonyms:
Definition: A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MYO18B gene on chromosome 22q12. https://www.ncbi.nlm.nih.gov/pubmed/25748484
References:
Ontology: Human Disease   (DOID:0080592)
OTHER Klippel-Feil syndrome 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYO18B Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism 616549
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None