Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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 ..Perceptual Disorders (D010468)
Child Nodes:
........Agnosia (D000377) 4
........Alice in Wonderland Syndrome (D062026)
........Allesthesia (D066190)
........Auditory Perceptual Disorders (D001308) 1
........Hallucinations (D006212)
........Illusions (D007088)
........Phantom Limb (D010591)
........Synesthesia (C562460)
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:	8784
Name:	Perceptual Disorders
Definition:	Cognitive disorders characterized by an impaired ability to perceive the nature of objects or concepts through use of the sense organs. These include spatial neglect syndromes, where an individual does not attend to visual, auditory, or sensory stimuli presented from one side of the body.
Alternative IDs:
ParentIDs:	MESH:D019954
TreeNumbers:	C10.597.606.762 \|C23.888.592.604.764
Synonyms:	Discrimination Disorder, Somatosensory \|Discrimination Disorders, Somatosensory \|Hemisensory Neglect \|Hemisensory Neglects \|Hemispatial Neglect \|Hemispatial Neglects \|Neglect, Hemisensory \|Neglect, Hemispatial \|Neglect, Sensory \|Neglects, Hemisensory \|Perceptual D
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D010468 MeSH: D010468 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants