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 ..Confusion (D003221)
Child Nodes:
........Carnitine Acetyltransferase Deficiency (C563249)
........Delirium (D003693)
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:	2589
Name:	Confusion
Definition:	A mental state characterized by bewilderment, emotional disturbance, lack of clear thinking, and perceptual disorientation.
Alternative IDs:
ParentIDs:	MESH:D019954
TreeNumbers:	C10.597.606.337 \|C23.888.592.604.339
Synonyms:	Bewilderment \|Confusional State \|Confusional States \|Confusion, Post Ictal \|Confusion, Post-Ictal \|Confusion, Reactive \|Disorientation \|Post-Ictal Confusion \|Reactive Confusion \|State, Confusional \|States, Confusional
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D003221 MeSH: D003221 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants