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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: Sleep Disorders (D012893)
..Starting node ..Parasomnias (D020447)
Child Nodes:
........Nocturnal Myoclonus Syndrome (D020189)
........Nocturnal Paroxysmal Dystonia (D020183)
........REM Sleep Parasomnias (D020923) 2
........Restless Legs Syndrome (D012148) 2
........Sleep Arousal Disorders (D020921) 3
........Sleep Bruxism (D020186) 1
........Sleep-Wake Transition Disorders (D020922)
Sister Nodes:
..Autosomal Dominant Lateral Temporal Lobe Epilepsy (C537297)
..Dyssomnias (D020920) 27
..Parasomnias (D020447) 15
..Sleep Deprivation (D012892)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8630
Name:	Parasomnias
Definition:	Movements or behaviors associated with sleep, sleep stages, or partial arousals from sleep that may impair sleep maintenance. Parasomnias are generally divided into four groups: arousal disorders, sleep-wake transition disorders, parasomnias of REM sleep, and nonspecific parasomnias. (From Thorpy, Sleep Disorders Medicine, 1994, p191)
Alternative IDs:
ParentIDs:	MESH:D012893
TreeNumbers:	C10.886.659 \|F03.870.664
Synonyms:	Benign Neonatal Sleep Myoclonus \|Drunkennesses, Sleep \|Drunkenness, Sleep \|Myoclonus, Benign Neonatal Sleep \|Neonatal Sleep Myoclonus, Benign \|Parasomnia \|Paroxysm, Sleep Sensory \|Paroxysms, Sleep Sensory \|Sensory Paroxysm, Sleep \|Sensory Paroxysms, Sleep \|Sleep D
Slim Mappings:	Mental disorder\|Nervous system disease
Reference:	MedGen: D020447 MeSH: D020447 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants