Dementia

Symptom Information:

Symptom ID: HPO:0000726
Synonyms:
Dementia, progressive [HPO:0000726]
Progressive dementia [HPO:0000726]
Dementia (disorder) [Orphanet:43520]
Dementia [Orphanet:43520]
Demented [Orphanet:43520]
Dementia [OMIM:Dementia]
Dementia, progressive [OMIM:Dementia, progressive]
Progressive dementia [OMIM:Progressive dementia]
Psychic/psychomotor regression/dementia/intellectual decline [Orphanet:43520]
Dementia [MedDRA:10012267]
Amentia [MedDRA:10012267]
Brain failure, chronic [MedDRA:10012267]
Brain syndrome chronic [MedDRA:10012267]
Chronic brain failure [MedDRA:10012267]
Chronic brain syndrome [MedDRA:10012267]
Demented [MedDRA:10012267]
Dementia acquired [MedDRA:10012267]
Dementia aggravated [MedDRA:10012267]
Dementia due to Creutzfeldt-Jacob disease [MedDRA:10012267]
Dementia due to Creutzfeld-Jakob disease [MedDRA:10012267]
Dementia due to general medical condition [MedDRA:10012267]
Dementia due to head trauma [MedDRA:10012267]
Dementia due to Huntington's disease [MedDRA:10012267]
Dementia due to Jakob's disease [MedDRA:10012267]
Dementia due to multiple aetiologies [MedDRA:10012267]
Dementia due to multiple etiologies [MedDRA:10012267]
Dementia due to other general medical condition [MedDRA:10012267]
Dementia due to other general medical conditions [MedDRA:10012267]
Dementia due to Parkinson's disease [MedDRA:10012267]
Dementia in conditions classified elsewhere [MedDRA:10012267]
Dementia NOS [MedDRA:10012267]
Dementia NOS aggravated [MedDRA:10012267]
Disorder brain (chronic) [MedDRA:10012267]
Drug-induced dementia [MedDRA:10012267]
Mental disorder post brain damage [MedDRA:10012267]
Organic brain failure [MedDRA:10012267]
Other specified organic brain syndromes (chronic) [MedDRA:10012267]
Post-traumatic dementia [MedDRA:10012267]
Secondary dementia [MedDRA:10012267]
Syndrome brain chronic [MedDRA:10012267]
Toxic dementia [MedDRA:10012267]
Unspecified organic brain syndrome (chronic) [MedDRA:10012267]
Dementia (5%) [OMIM:Dementia (5%)]
Dementia (<20%) [OMIM:Dementia (<20%)]
Dementia (in some patients) [OMIM:Dementia (in some patients)]
Dementia (later onset) [OMIM:Dementia (later onset)]
Dementia (later-onset) [OMIM:Dementia (later-onset)]
Dementia (onset in fifth decade) [OMIM:Dementia (onset in fifth decade)]
Dementia (rare) [OMIM:Dementia (rare)]
Dementia (subtype 3A) [OMIM:Dementia (subtype 3A)]
Dementia, progressive (more common in males) [OMIM:Dementia, progressive (more common in males)]
No dementia [OMIM:No dementia]
Dementia (excl Alzheimer's type) [MedDRA:10012268]
Quality:
Cross references:
Orphanet:43520 "Psychic/psychomotor regression/dementia/intellectual decline" [Orphanet:43520]
OMIM: "Dementia" [OMIM:Dementia]
OMIM: "Dementia, progressive" [OMIM:Dementia, progressive]
OMIM: "Progressive dementia" [OMIM:Progressive dementia]
OMIM: "Dementia (5%)" [OMIM:Dementia (5%)]
OMIM: "Dementia (<20%)" [OMIM:Dementia (<20%)]
OMIM: "Dementia (in some patients)" [OMIM:Dementia (in some patients)]
OMIM: "Dementia (later onset)" [OMIM:Dementia (later onset)]
OMIM: "Dementia (later-onset)" [OMIM:Dementia (later-onset)]
OMIM: "Dementia (onset in fifth decade)" [OMIM:Dementia (onset in fifth decade)]
OMIM: "Dementia (rare)" [OMIM:Dementia (rare)]
OMIM: "Dementia (subtype 3A)" [OMIM:Dementia (subtype 3A)]
OMIM: "Dementia, progressive (more common in males)" [OMIM:Dementia, progressive (more common in males)]
OMIM: "No dementia" [OMIM:No dementia]
UMLS:C0497327 "Dementia" [HPO:0000726]
UMLS:C0497327 "Dementia" [Orphanet:43520]
UMLS:C0860630 "Demented" [Orphanet:43520]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
MedDRA Dementia NEC
HPO         Mental deterioration
MedDRA Mental impairment disorders
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)
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)