Search Ontology:
Human Disease

Klippel-Feil syndrome 4

Term ID
DOID:0080592
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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