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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 ..Memory Disorders (D008569)
Child Nodes:
........Amnesia (D000647) 6
........Korsakoff Syndrome (D020915)
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:	6937
Name:	Memory Disorders
Definition:	Disturbances in registering an impression, in the retention of an acquired impression, or in the recall of an impression. Memory impairments are associated with DEMENTIA; CRANIOCEREBRAL TRAUMA; ENCEPHALITIS; ALCOHOLISM (see also ALCOHOL AMNESTIC DISORDER); SCHIZOPHRENIA; and other conditions.
Alternative IDs:
ParentIDs:	MESH:D019954
TreeNumbers:	C10.597.606.525 \|C23.888.592.604.529
Synonyms:	Age-Related Memory Disorder \|Age Related Memory Disorders \|Age-Related Memory Disorders \|Cognitive Retention Disorder \|Cognitive Retention Disorders \|Deficit, Memory \|Deficits, Memory \|Memory Deficit \|Memory Deficits \|Memory Disorder \|Memory Disorder, Age-Related \|
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D008569 MeSH: D008569 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants