Dementia
Symptom Information:
Symptom ID: | HPO:0000726 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Cognitive impairment(HPO:0100543) Mental deterioration(HPO:0001268) Dementia(HPO:0000726) MedDRA: Nervous system disorders(MedDRA:10029205) Mental impairment disorders(MedDRA:10057167) Dementia(HPO:0000726) |
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Database Frequency: | 131 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALZHEIMER DISEASE 10 | (OMIM:609636) |
ALZHEIMER DISEASE 2 | (OMIM:104310) |
ALZHEIMER DISEASE 3 | (OMIM:607822) |
ALZHEIMER DISEASE 4 | (OMIM:606889) |
ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL | (OMIM:502500) |
AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA | (OMIM:205200) |
ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT | (OMIM:206570) |
ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA | (OMIM:208700) |
ATTRV122I amyloidosis | (Orphanet:85451) |
Aceruloplasminemia | (Orphanet:48818) |
Adrenomyeloneuropathy | (Orphanet:139399) |
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
Alpers syndrome | (Orphanet:726) |
Amelo-cerebro-hypohidrotic syndrome | (Orphanet:1946) |
Amyotrophic lateral sclerosis-parkinsonism-dementia complex | (Orphanet:90020) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Atypical progressive supranuclear palsy | (Orphanet:99750) |
Autosomal dominant popliteal pterygium syndrome | (Orphanet:1300) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 21 | (Orphanet:101001) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 | (OMIM:615007) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 | (OMIM:615483) |
Beta-propeller protein-associated neurodegeneration | (Orphanet:329284) |
CADASIL | (Orphanet:136) |
CARASIL | (Orphanet:199354) |
CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY | (OMIM:607674) |
CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE | (OMIM:302700) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
CHOREA, BENIGN HEREDITARY | (OMIM:118700) |
CHOREOATHETOSIS, FAMILIAL INVERTED | (OMIM:118750) |
CLN13 disease | (Orphanet:352709) |
CLN3 disease | (Orphanet:228346) |
CLN4A disease | (Orphanet:228340) |
CLN4B disease | (Orphanet:228343) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Cardiomyopathy, dilated, 1U | (OMIM:613694) |
Cardiomyopathy, dilated, 1V | (OMIM:613697) |
Cerebellar ataxia - hypogonadism | (Orphanet:1173) |
Cerebellar ataxia-deafness-narcolepsy syndrome | (Orphanet:314404) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Choreoacanthocytosis | (Orphanet:2388) |
Creutzfeldt-Jakob disease | (Orphanet:204) |
Cystinosis | (Orphanet:213) |
DEMENTIA, LEWY BODY | (OMIM:127750) |
DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES | (OMIM:125320) |
Dentatorubral pallidoluysian atrophy | (Orphanet:101) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 8 | (OMIM:616230) |
Early-onset autosomal dominant Alzheimer disease | (Orphanet:1020) |
Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
Familial amyloid polyneuropathy | (Orphanet:85447) |
Familial dementia, British type | (Orphanet:97345) |
Familial dementia, Danish type | (Orphanet:97346) |
Familial encephalopathy with neuroserpin inclusion bodies | (Orphanet:85110) |
Fatal familial insomnia | (Orphanet:466) |
Flynn-Aird syndrome | (Orphanet:2047) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
GM2-gangliosidosis, AB variant | (Orphanet:309246) |
GORDON HOLMES SYNDROME | (OMIM:212840) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
Gräsbeck-Imerslund disease | (Orphanet:35858) |
HERNS syndrome | (Orphanet:63261) |
HYDROCEPHALUS, NORMAL-PRESSURE | (OMIM:236690) |
HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION | (OMIM:607236) |
Hereditary cerebral hemorrhage with amyloidosis, Dutch type | (Orphanet:100006) |
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type | (Orphanet:100008) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Huntington disease | (Orphanet:399) |
Huntington disease-like 1 | (Orphanet:157941) |
Huntington disease-like 2 | (Orphanet:98934) |
INTERNAL CAROTID ARTERIES, HYPOPLASIA OF | (OMIM:243100) |
Inherited Creutzfeldt-Jakob disease | (Orphanet:282166) |
Juvenile Huntington disease | (Orphanet:248111) |
Kearns-Sayre syndrome | (Orphanet:480) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
LEBER OPTIC ATROPHY AND DYSTONIA | (OMIM:500001) |
LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE | (OMIM:615889) |
Lafora disease | (Orphanet:501) |
Leber plus disease | (Orphanet:99718) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA | (OMIM:600333) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Menkes disease | (Orphanet:565) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
NARP syndrome | (Orphanet:644) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IE | (OMIM:614116) |
NIEMANN-PICK DISEASE, TYPE C1 | (OMIM:257220) |
NIEMANN-PICK DISEASE, TYPE C2 | (OMIM:607625) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Neuroferritinopathy | (Orphanet:157846) |
Niemann-Pick disease type C | (Orphanet:646) |
Norrie disease | (Orphanet:649) |
OLIVOPONTOCEREBELLAR ATROPHY V | (OMIM:164700) |
OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA | (OMIM:311150) |
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE | (OMIM:600116) |
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT | (OMIM:605543) |
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:605909) |
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT | (OMIM:607060) |
PARKINSON DISEASE, LATE-ONSET | (OMIM:168600) |
PRESENILE DEMENTIA, KRAEPELIN TYPE | (OMIM:176600) |
PRESENILIN 1 | (OMIM:104311) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Progressive supranuclear palsy - parkinsonism | (Orphanet:240085) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA | (OMIM:182830) |
SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES | (OMIM:606688) |
Sneddon syndrome | (Orphanet:820) |
Spinocerebellar ataxia type 10 | (Orphanet:98761) |
Spinocerebellar ataxia type 12 | (Orphanet:98762) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Tay-Sachs disease | (Orphanet:845) |
Wilson disease | (Orphanet:905) |
Wolfram syndrome | (Orphanet:3463) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |
X-linked spinocerebellar ataxia type 4 | (Orphanet:85292) |
Xeroderma pigmentosum complementation group F | (Orphanet:276264) |