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Mobius syndrome

Disease Summary
Associated Targets (3)
Tbio

3


Explore Associated Targets
Mondo Description Moebius syndrome is a very rare congenital cranial dysinnervation disorder characterized by complete or incomplete facial paralysis in association with bilateral palsy of the abducens nerve causing impairment of ocular abduction. The syndrome also includes various other congenital anomalies.
Disease Ontology Description A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s).
Mondo Term and Equivalent IDs
MONDO:0008006:  Mobius syndrome
EFO:1001046: 
GARD:0008549: 
MESH:D020331: 
NCIT:C84893: 
Orphanet:570: 
SCTID:89444000: 
UMLS:C0221060: 
UMLS:C0853240: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)