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Summary Literature (0)
DOID:13501 - Mobius syndrome

Disease Ontology Definition:A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s).

Synonyms: Moebius congenital oculofacial paralysis, Oromandibular-limb hypogenesis spectrum

Xenbase Genes : plxnd1, rev3l

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008006 - Mobius syndrome


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): facial nerve disease (is_a)