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Disease Ontology Browser
Klippel-Feil syndrome 4 (DOID:0080592)
Alliance: disease page
Alt IDs: OMIM:616549, ORDO:447974
Definition: A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MYO18B gene on chromosome 22q12.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory