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: Neurobehavioral Manifestations (D019954)
..Starting node ..Lethargy (D053609)
Child Nodes:
Sister Nodes:
..Anhedonia (D059445)
..Apraxias (D001072) 10
..Catatonia (D002389) 1
..Communication Disorders (D003147) 57
..Confusion (D003221) 2
..Consciousness Disorders (D003244) 11
..Intellectual Disability (D008607) 579
..Lethargy (D053609)
..Memory Disorders (D008569) 7
..Perceptual Disorders (D010468) 13
..Psychomotor Disorders (D011596) 34
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6329
Name:	Lethargy
Definition:	A general state of sluggishness, listless, or uninterested, with being tired, and having difficulty concentrating and doing simple tasks. It may be related to DEPRESSION or DRUG ADDICTION.
Alternative IDs:
ParentIDs:	MESH:D019954
TreeNumbers:	C10.597.606.441 \|C23.888.592.604.444
Synonyms:
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D053609 MeSH: D053609 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants