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Disease Ontology Browser
Mobius syndrome (DOID:13501)
Alliance: disease page
Synonyms: 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory