You are using an outdated browser. Please upgrade your browser to improve your experience.

opsoclonus-myoclonus syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Opsoclonus myoclonus syndrome (OMS) is a rare neuroinflammatory disease of paraneoplastic, parainfectious or idiopathic origin, characterized by opsoclonus, myoclonus, ataxia, and behavioral and sleep disorders.
Mondo Term and Equivalent IDs
MONDO:0015247:  opsoclonus-myoclonus syndrome
EFO:1001383: 
GARD:0010009: 
MESH:D053578: 
NCIT:C4686: 
Orphanet:1183: 
SCTID:230350000: 
UMLS:C0393626: