Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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, Intrinsic (D020919)
..Starting node ..Disorders of Excessive Somnolence (D006970)
Child Nodes:
........Hyper-Beta-Alaninemia (C562684)
........Hypersomnolence, Idiopathic (D020177)
........Kleine-Levin Syndrome (D017593)
........Narcolepsy (D009290) 5
Sister Nodes:
..Disorders of Excessive Somnolence (D006970) 9
..Nocturnal Myoclonus Syndrome (D020189)
..Restless Legs Syndrome (D012148) 2
..Sleep Apnea Syndromes (D012891) 5
..Sleep Initiation and Maintenance Disorders (D007319) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3406
Name:	Disorders of Excessive Somnolence
Definition:	Disorders characterized by hypersomnolence during normal waking hours that may impair cognitive functioning. Subtypes include primary hypersomnia disorders (e.g., IDIOPATHIC HYPERSOMNOLENCE; NARCOLEPSY; and KLEINE-LEVIN SYNDROME) and secondary hypersomnia disorders where excessive somnolence can be attributed to a known cause (e.g., drug affect, MENTAL DISORDERS, and SLEEP APNEA SYNDROME). (From J Neurol Sci 1998 Jan 8;153(2):192-202; Thorpy, Principles and Practice of Sleep Medicine, 2nd ed, p320)
Alternative IDs:
ParentIDs:	MESH:D020919
TreeNumbers:	C10.886.425.800.200 \|F03.870.400.800.200
Synonyms:	DOES (Disorders of Excessive Somnolence) \|DOESs (Disorders of Excessive Somnolence) \|Excessive Somnolence Disorder \|Excessive Somnolence Disorders \|Hypersomnia \|Hypersomnia, Recurrent \|Hypersomnias \|Hypersomnias, Recurrent \|Hypersomnolence \|Hypersomnolence Disord
Slim Mappings:	Mental disorder\|Nervous system disease
Reference:	MedGen: D006970 MeSH: D006970 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants