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: Brain Diseases (D001927)
Parent Node: Dementia (D003704)
..Starting node ..Kluver-Bucy Syndrome (D020232)
Child Nodes:
........Bilateral temporal lobe disorder (C538521)
Sister Nodes:
..AIDS Dementia Complex (D015526)
..Alzheimer Disease (D000544) 24
..Amyloidosis, Cerebral, with Spongiform Encephalopathy (C535800)
..Amyotrophic Lateral Sclerosis, Juvenile, with Dementia (C565956)
..AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1 (OMIM:105500)
..Aphasia, Primary Progressive (D018888) 1
..Ataxia with Myoclonic Epilepsy and Presenile Dementia (C565933)
..Creutzfeldt-Jakob Syndrome (D007562) 3
..Dementia, familial Danish (C538209)
..Dementia, Vascular (D015140) 3
..Dementia/Parkinsonism With Non-Alzheimer Amyloid Plaques (C565115)
..Diffuse Neurofibrillary Tangles with Calcification (D055956)
..Frontotemporal Lobar Degeneration (D057174) 12
..Huntington Disease (D006816) 3
..Huntington Disease-Like 2 (C564708)
..Jensen syndrome (C537568)
..Kluver-Bucy Syndrome (D020232) 1
..Kohlschutter Tonz syndrome (C537213)
..Lewy Body Disease (D020961) 3
..MAST Syndrome (C565409)
..Motor Neuron Disease with Dementia and Ophthalmoplegia (C563954)
..Presenile dementia, Kraepelin type (C535273)
..Spastic Paraplegia, Optic Atrophy, And Dementia (C566679)
..Wright Dyck syndrome (C536749)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6117
Name:	Kluver-Bucy Syndrome
Definition:	A neurobehavioral syndrome associated with bilateral medial temporal lobe dysfunction. Clinical manifestations include oral exploratory behavior; tactile exploratory behavior; hypersexuality; BULIMIA; MEMORY DISORDERS; placidity; and an inability to recognize objects or faces. This disorder may result from a variety of conditions, including CRANIOCEREBRAL TRAUMA; infections; ALZHEIMER DISEASE; PICK DISEASE OF THE BRAIN; and CEREBROVASCULAR DISORDERS.
Alternative IDs:
ParentIDs:	MESH:D001927\|MESH:D003704
TreeNumbers:	C10.228.140.380.326 \|C10.228.140.646 \|F03.087.400.431
Synonyms:	Kluver Bucy Syndrome \|Syndrome, Kluver-Bucy \|Temporal Lobectomy Behavior Syndrome
Slim Mappings:	Mental disorder\|Nervous system disease
Reference:	MedGen: D020232 MeSH: D020232 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants