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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).

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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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory