Moebius syndrome

Summary

DOID:13501 - Moebius 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: Mobius syndrome, Moebius congenital oculofacial paralysis, Oromandibular-limb hypogenesis spectrum,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: plxnd1, rev3l

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008006 - Mobius syndrome

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): autosomal dominant disease (is_a), facial nerve disease (is_a)