| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Opsoclonus myoclonus syndrome (OMS) is a rare pediatric brain inflammatory disease of paraneoplastic, parainfectious or idiopathic origin, characterized by opsoclonus, myoclonus, ataxia and behavioural and sleep disorders. (Orphanet Rare Disease Ontology, Orphanet_1183) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D053578 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Opsoclonus-Myoclonus Syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| POMC | proopiomelanocortin | 2.88009 |
