Mental deterioration
Symptom Information:
Symptom ID: | HPO:0001268 | ||||||||||||||||||||||||||||||||
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) Cognitive impairment(HPO:0100543) Mental deterioration(HPO:0001268) MedDRA: Nervous system disorders(MedDRA:10029205) Mental impairment disorders(MedDRA:10057167) Mental deterioration(HPO:0001268) |
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Database Frequency: | 88 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
ALTERNATING HEMIPLEGIA OF CHILDHOOD 1 | (OMIM:104290) |
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 | (OMIM:614820) |
Aceruloplasminemia | (Orphanet:48818) |
Adrenomyeloneuropathy | (Orphanet:139399) |
Adult polyglucosan body disease | (Orphanet:206583) |
Adult-onset dystonia-parkinsonism | (Orphanet:199351) |
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
Alternating hemiplegia of childhood | (Orphanet:2131) |
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 | (OMIM:213600) |
Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
Bilateral striopallidodentate calcinosis | (Orphanet:1980) |
CADASIL | (Orphanet:136) |
CLN11 disease | (Orphanet:314629) |
CLN13 disease | (Orphanet:352709) |
CLN6 disease | (Orphanet:228363) |
CLN7 disease | (Orphanet:228366) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Coats plus syndrome | (Orphanet:313838) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
Dravet syndrome | (Orphanet:33069) |
Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY | (OMIM:615924) |
EPILEPSY, PROGRESSIVE MYOCLONIC 7 | (OMIM:616187) |
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 | (OMIM:613832) |
Familial encephalopathy with neuroserpin inclusion bodies | (Orphanet:85110) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 3 | (Orphanet:77261) |
HERNS syndrome | (Orphanet:63261) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Huntington disease | (Orphanet:399) |
Huntington disease-like 1 | (Orphanet:157941) |
Huntington disease-like 3 | (Orphanet:157946) |
Hurler syndrome | (Orphanet:93473) |
KRABBE DISEASE | (OMIM:245200) |
KURU, SUSCEPTIBILITY TO | (OMIM:245300) |
Knobloch syndrome | (Orphanet:1571) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS | (OMIM:614561) |
Lafora disease | (Orphanet:501) |
Leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation | (Orphanet:137898) |
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A | (OMIM:613925) |
MEGDEL syndrome | (Orphanet:352328) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY | (OMIM:249900) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Menkes disease | (Orphanet:565) |
Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B | (OMIM:610217) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
NIEMANN-PICK DISEASE, TYPE C1 | (OMIM:257220) |
NIEMANN-PICK DISEASE, TYPE C2 | (OMIM:607625) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Niemann-Pick disease type C | (Orphanet:646) |
OPTICOCOCHLEODENTATE DEGENERATION | (OMIM:258700) |
PARKINSON DISEASE 20, EARLY-ONSET | (OMIM:615530) |
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT | (OMIM:607060) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 | (OMIM:610489) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 | (OMIM:610475) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Primary pigmented nodular adrenocortical disease | (Orphanet:189439) |
Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Sneddon syndrome | (Orphanet:820) |
Spinocerebellar ataxia type 14 | (Orphanet:98763) |
Spinocerebellar ataxia type 7 | (Orphanet:94147) |
Unverricht-Lundborg disease | (Orphanet:308) |
Wolfram syndrome | (Orphanet:3463) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |
Xeroderma pigmentosum complementation group A | (Orphanet:276249) |
Xeroderma pigmentosum complementation group D | (Orphanet:276258) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |
Young adult-onset Parkinsonism | (Orphanet:2828) |