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: Delirium, Dementia, Amnestic, Cognitive Disorders (D019965)
Parent Node: Neurobehavioral Manifestations (D019954)
..Starting node ..Consciousness Disorders (D003244)
Child Nodes:
........Unconsciousness (D014474) 10
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:	2680
Name:	Consciousness Disorders
Definition:	Organic mental disorders in which there is impairment of the ability to maintain awareness of self and environment and to respond to environmental stimuli. Dysfunction of the cerebral hemispheres or brain stem RETICULAR FORMATION may result in this condition.
Alternative IDs:
ParentIDs:	MESH:D019954\|MESH:D019965
TreeNumbers:	C10.597.606.358 \|C23.888.592.604.359 \|F03.087.300
Synonyms:	Altered Level of Consciousness \|Consciousness Disorder \|Consciousness, Level Altered \|Consciousness, Level Depressed \|Depressed Level of Consciousness \|Semiconsciousness
Slim Mappings:	Mental disorder\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: D003244 MeSH: D003244 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants