About   Help   FAQ
Disease Ontology Browser
Moebius syndrome (DOID:13501)
Alliance: disease page
Synonyms: Mobius syndrome; Moebius congenital oculofacial paralysis; Oromandibular-limb hypogenesis spectrum
Alt IDs: OMIM:157900, ICD10CM:Q87.0, MESH:D020331, NCI:C84893, UMLS_CUI:C0221060
Definition: A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s).

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory