Memory impairment
Symptom Information:
Symptom ID: | HPO:0002354 | |||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||
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) Memory impairment(HPO:0002354) MedDRA: Nervous system disorders(MedDRA:10029205) Mental impairment disorders(MedDRA:10057167) Memory impairment(HPO:0002354) |
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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) |