About   Help   FAQ
Disease Ontology Browser
Klippel-Feil syndrome (DOID:10426)
Synonyms: autosomal dominant Klippel-Feil syndrome; congenital dystrophia brevicollis; congenital synostosis of cervical vertebrae; Klippel-Feil and Turner syndrome; Klippel-Feil deformity, deafness and facial asymmetry
Alt IDs: OMIM:118100, OMIM:214300, OMIM:613702, DOID:14747, ICD10CM:Q76.1, ICD9CM:756.16, MESH:D007714, NCI:C98967, ORDO:2345, UMLS_CUI:C0022738
Definition: A physical disorder that has_material_basis_in abnormal segmentation of the vertebra during fetal development which results_in fusion located_in cervical vertebra.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
03/14/2017
MGI 6.08
The Jackson Laboratory