Confusion
Symptom Information:
Symptom ID: | HPO:0001289 | |||||||||||||||||||||||||||||||||||||||||||||
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) Reduced consciousness/confusion(HPO:0004372) Confusion(HPO:0001289) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Cortical dysfunction NEC(MedDRA:10011168) Confusion(HPO:0001289) Neurological signs and symptoms NEC(MedDRA:10029306) Confusion(HPO:0001289) |
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Database Frequency: | 36 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alpha-mannosidosis | (Orphanet:61) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Biotin-responsive basal ganglia disease | (Orphanet:65284) |
CADASIL | (Orphanet:136) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Carnitine uptake deficiency | (Orphanet:158) |
Citrullinemia type II | (Orphanet:247585) |
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency | (Orphanet:93583) |
Creutzfeldt-Jakob disease | (Orphanet:204) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Encephalopathy due to GLUT1 deficiency | (Orphanet:71277) |
Familial atrial myxoma | (Orphanet:615) |
Familial or sporadic hemiplegic migraine | (Orphanet:569) |
Gräsbeck-Imerslund disease | (Orphanet:35858) |
Hereditary coproporphyria | (Orphanet:79273) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Inherited Creutzfeldt-Jakob disease | (Orphanet:282166) |
Kleine-Levin syndrome | (Orphanet:33543) |
MELAS | (Orphanet:550) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 | (OMIM:141500) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IE | (OMIM:614116) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION | (OMIM:172500) |
Pellagra-like skin rash-neurological manifestations | (Orphanet:2837) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |
WERNICKE-KORSAKOFF SYNDROME | (OMIM:277730) |
Wolfram syndrome | (Orphanet:3463) |