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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Myoclonus (D009207)
Parent Node: Ocular Motility Disorders (D015835)
Parent Node: Paraneoplastic Syndromes, Nervous System (D020361)
..Starting node ..Opsoclonus-Myoclonus Syndrome (D053578)
Child Nodes:
........Infantile polymyoclonus (C535524)
Sister Nodes:
..Anti-N-Methyl-D-Aspartate Receptor Encephalitis (D060426)
..Lambert-Eaton Myasthenic Syndrome (D015624)
..Limbic Encephalitis (D020363) 1
..Myelitis, Transverse (D009188) 1
..Opsoclonus-Myoclonus Syndrome (D053578) 1
..Paraneoplastic Cerebellar Degeneration (D020362)
..Paraneoplastic Polyneuropathy (D020364)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8270
Name:	Opsoclonus-Myoclonus Syndrome
Definition:	A neurological condition that is characterized by uncontrolled rapid irregular movements of the eye (OPSOCLONUS) and the muscle (MYOCLONUS) causing unsteady, trembling gait. It is also known as dancing eyes-dancing feet syndrome and is often associated with neoplasms, viral infections, or autoimmune disorders involving the nervous system.
Alternative IDs:
ParentIDs:	MESH:D009207\|MESH:D015835\|MESH:D020361
TreeNumbers:	C04.588.614.550.600 \|C04.730.856.596 \|C10.228.758.500 \|C10.292.562.831 \|C10.574.781.662 \|C10.597.350.500.500 \|C11.590.725
Synonyms:	Dancing Eyes Dancing Feet Syndrome \|Dancing Eyes-Dancing Feet Syndrome \|Dancing Eyes, Dancing Feet Syndrome \|Infants Myoclonic Encephalopathies \|Infants Myoclonic Encephalopathy \|Kinsbourne Syndrome \|Myoclonic Encephalopathy of Infants \|Myoclonus, Opsoclonus \|Op
Slim Mappings:	Cancer\|Eye disease\|Nervous system disease
Reference:	MedGen: D053578 MeSH: D053578 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants