Memory impairment

Symptom Information:

Symptom ID: HPO:0002354
Synonyms:
Forgetfulness [HPO:0002354]
Memory loss [HPO:0002354]
Amnesia [Orphanet:43530]
Amnesia (finding) [Orphanet:43530]
Memory Loss [Orphanet:43530]
Forgetfulness [OMIM:Forgetfulness]
Memory impairment [OMIM:Memory impairment]
Memory loss [OMIM:Memory loss]
Troubles of memory/amnesia/hypermnesia [Orphanet:43530]
Memory loss of [Orphanet:43530]
Amnesia [MedDRA:10001949]
Amnesia NEC [MedDRA:10001949]
Amnesia transient [MedDRA:10001949]
Long-term memory loss [MedDRA:10001949]
Losing memory in mornings [MedDRA:10001949]
Loss of memory [MedDRA:10001949]
Loss of memory ability [MedDRA:10001949]
Memory loss [MedDRA:10001949]
Memory loss of [MedDRA:10001949]
Memory loss transient [MedDRA:10001949]
Partial loss of memory [MedDRA:10001949]
Short-term memory loss [MedDRA:10001949]
Total loss of memory [MedDRA:10001949]
Amnesia aggravated [MedDRA:10001949]
Global amnesia [MedDRA:10001949]
Hypermnesia [Orphanet:43530]
Hypermnesia (finding) [Orphanet:43530]
Memory loss (excl dementia) [MedDRA:10027177]
Memory impairment [MedDRA:10027175]
Quality:
Cross references:
Orphanet:43530 "Troubles of memory/amnesia/hypermnesia" [Orphanet:43530]
OMIM: "Forgetfulness" [OMIM:Forgetfulness]
OMIM: "Memory impairment" [OMIM:Memory impairment]
OMIM: "Memory loss" [OMIM:Memory loss]
UMLS:C0542476 "Forgetfulness" [HPO:0002354]
UMLS:C0002622 "Amnesia" [Orphanet:43530]
UMLS:C0751295 "Memory Loss" [Orphanet:43530]
UMLS:C0233804 "Hypermnesia" [Orphanet:43530]
Is a (Direct Parents):
MedDRA Mental impairment disorders
HPO         Abnormality of higher mental function
Orphanet Functional anomalies of the nervous system
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)
                Memory impairment(HPO:0002354)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Mental impairment disorders(MedDRA:10057167)
       Memory impairment(HPO:0002354)
Database Frequency: 63 / 7739
Resource:

All diseases associated with this symptom:

ALZHEIMER DISEASE 10 (OMIM:609636)
ALZHEIMER DISEASE 3 (OMIM:607822)
Aceruloplasminemia (Orphanet:48818)
Adiposis dolorosa (Orphanet:36397)
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (Orphanet:313808)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Autosomal dominant spastic ataxia 1 (Orphanet:251282)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Autosomal recessive spastic paraplegia type 14 (Orphanet:100995)
Autosomal recessive spastic paraplegia type 7 (Orphanet:99013)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
Bardet-Biedl syndrome 7 (OMIM:615984)
Behavioral variant of frontotemporal dementia (Orphanet:275864)
Behçet disease (Orphanet:117)
Benign familial infantile seizures (Orphanet:306)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
CACH syndrome (Orphanet:135)
CADASIL (Orphanet:136)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cerebellar ataxia-deafness-narcolepsy syndrome (Orphanet:314404)
Choreoacanthocytosis (Orphanet:2388)
Classical phenylketonuria (Orphanet:79254)
Classical progressive supranuclear palsy (Orphanet:240071)
Congenital or early infantile CACH syndrome (Orphanet:157713)
Cree leukoencephalopathy (Orphanet:99854)
Creutzfeldt-Jakob disease (Orphanet:204)
Crigler-Najjar syndrome (Orphanet:205)
Crigler-Najjar syndrome type 1 (Orphanet:79234)
Cystinosis (Orphanet:213)
Cystinuria (Orphanet:214)
Cystinuria type B (Orphanet:93613)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Gerstmann-Straussler-Scheinker syndrome (Orphanet:356)
Hereditary cerebral hemorrhage with amyloidosis, Iowa type (Orphanet:324708)
Hypernychthemeral syndrome (Orphanet:73267)
Inherited Creutzfeldt-Jakob disease (Orphanet:282166)
Juvenile neuronal ceroid lipofuscinosis (Orphanet:79264)
Juvenile or adult CACH syndrome (Orphanet:157719)
Late infantile CACH syndrome (Orphanet:157716)
Lipoid proteinosis (Orphanet:530)
Lyme disease (Orphanet:91546)
MELAS (Orphanet:550)
MYXEDEMA (OMIM:255900)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
NEUROPATHY, HEREDITARY SENSORY, TYPE IE (OMIM:614116)
Narcolepsy-cataplexy (Orphanet:2073)
Nasu-Hakola disease (Orphanet:2770)
Neurofibromatosis type 1 (Orphanet:636)
Non-polyposis Turcot syndrome (Orphanet:99817)
Ovarioleukodystrophy (Orphanet:99853)
Posterior cortical atrophy (Orphanet:54247)
Progressive non-fluent aphasia (Orphanet:100070)
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 (OMIM:601104)
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 (OMIM:609454)
Scleroderma (Orphanet:801)
Sneddon syndrome (Orphanet:820)
Spinocerebellar ataxia type 14 (Orphanet:98763)
Spinocerebellar ataxia type 27 (Orphanet:98764)
WERNICKE-KORSAKOFF SYNDROME (OMIM:277730)
Waldenström macroglobulinemia (Orphanet:33226)
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE (OMIM:607259)