Disease browser and phenotype portal

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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: Dyssomnias (D020920)
Parent Node: Sleep Disorders (D012893)
..Starting node ..Sleep Deprivation (D012892)
Child Nodes:
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:	10310
Name:	Sleep Deprivation
Definition:	The state of being deprived of sleep under experimental conditions, due to life events, or from a wide variety of pathophysiologic causes such as medication effect, chronic illness, psychiatric illness, or sleep disorder.
Alternative IDs:
ParentIDs:	MESH:D012893\|MESH:D020920
TreeNumbers:	C10.886.425.175 \|C23.888.592.796.772 \|F03.870.400.099
Synonyms:	Deprivation, REM Sleep \|Deprivation, Sleep \|Deprivations, REM Sleep \|Deprivations, Sleep \|Fragmentation, Sleep \|Fragmentations, Sleep \|Insufficient Sleep Syndrome \|Insufficient Sleep Syndromes \|REM Sleep Deprivation \|REM Sleep Deprivations \|Sleep Deprivation, REM \|
Slim Mappings:	Mental disorder\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: D012892 MeSH: D012892 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants