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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: Catatonia (D002389)
Parent Node: Dementia (D003704)
..Starting node ..Presenile dementia, Kraepelin type (C535273)
Child Nodes:
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:

9264

Name:

Presenile dementia, Kraepelin type

Definition:

Alternative IDs:

ParentIDs:

MESH:D002389|MESH:D003704

TreeNumbers:

C10.228.140.380/C535273 |C10.597.606.115/C535273 |C23.888.592.604.115/C535273 |F03.087.400/C535273

Synonyms:

Catatonia of Kraepelin |Kraepelin disease

Slim Mappings:

Mental disorder|Nervous system disease|Signs and symptoms

Reference:

MedGen: C535273
MeSH: C535273
OMIM: 176600;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0000726	Dementia

Disease Causing ClinVar Variants