Confusion

Symptom Information:

Symptom ID: HPO:0001289
Synonyms:
Disorientation [HPO:0001289]
Disorientation [Orphanet:43470]
Disorientated (finding) [Orphanet:43470]
Confusional state (disorder) [Orphanet:43470]
Confusion [Orphanet:43470]
Confusion [OMIM:Confusion]
Disorientation [OMIM:Disorientation]
Obnubilation/coma/lethargia/desorientation [Orphanet:43470]
Confusional state [Orphanet:43470]
Disorientation [MedDRA:10013395]
Disorientated [MedDRA:10013395]
Nocturnal disorientation [MedDRA:10013395]
Orientation disturbed [MedDRA:10013395]
Temporal disorientation [MedDRA:10013395]
Spatial disorientation [MedDRA:10013395]
Temporospatial disorientation [MedDRA:10013395]
Confusional state [MedDRA:10010305]
Acute confusion state [MedDRA:10010305]
Acute confusional state [MedDRA:10010305]
Acute onset of confusion [MedDRA:10010305]
Bewilderment [MedDRA:10010305]
Confused [MedDRA:10010305]
Confusion [MedDRA:10010305]
Confusion nocturnal [MedDRA:10010305]
Confusion reversible [MedDRA:10010305]
Confusion state [MedDRA:10010305]
Confusional state (organic, acute or subacute) [MedDRA:10010305]
Mental confusion [MedDRA:10010305]
Nocturnal confusion [MedDRA:10010305]
Reactive confusion [MedDRA:10010305]
Subacute confusional state [MedDRA:10010305]
Toxic confusional state [MedDRA:10010305]
Confusion aggravated [MedDRA:10010305]
Confusion (later-onset) [OMIM:Confusion (later-onset)]
Disorientation (HCP) [OMIM:Disorientation (HCP)]
Delirium [MedDRA:10012218]
Acute confusion (finding) [Orphanet:43590]
Delirium (disorder) [Orphanet:43590]
Delirious (finding) [Orphanet:43590]
Acute confusional state [Orphanet:43590]
Delirium [Orphanet:43590]
Delirium/hallucination [Orphanet:43590]
Delirium [OMIM:Delirium]
Delirium (later-onset) [OMIM:Delirium (later-onset)]
consciousness disturbance
Quality:
Cross references:
Orphanet:43470 "Obnubilation/coma/lethargia/desorientation" [Orphanet:43470]
Orphanet:43590 "Delirium/hallucination" [Orphanet:43590]
OMIM: "Confusion" [OMIM:Confusion]
OMIM: "Disorientation" [OMIM:Disorientation]
OMIM: "Confusion (later-onset)" [OMIM:Confusion (later-onset)]
OMIM: "Disorientation (HCP)" [OMIM:Disorientation (HCP)]
OMIM: "Delirium" [OMIM:Delirium]
OMIM: "Delirium (later-onset)" [OMIM:Delirium (later-onset)]
UMLS:C1963086 "Confusion" [HPO:0001289]
UMLS:C0233407 "Disorientation" [Orphanet:43470]
UMLS:C0009676 "Confusion" [Orphanet:43470]
UMLS:C1285577 "Acute confusional state" [Orphanet:43590]
UMLS:C0011206 "Delirium" [Orphanet:43590]
Is a (Direct Parents):
Orphanet Sleep disturbance
HPO         Reduced consciousness/confusion
MedDRA Neurological signs and symptoms NEC
Orphanet Lethargy
Orphanet Hallucinations
MedDRA Cortical dysfunction NEC
Orphanet Behavioral abnormality
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)
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)