Hallucinations

Symptom Information:

Symptom ID: HPO:0000738
Synonyms:
Hallucination [HPO:0000738]
Hallucinations (finding) [Orphanet:43590]
Hallucinations [Orphanet:43590]
Hallucination [OMIM:Hallucination]
Hallucinations [OMIM:Hallucinations]
Delirium/hallucination [Orphanet:43590]
Hallucination [Orphanet:43590]
Hallucination [MedDRA:10019063]
Drug-induced hallucinosis [MedDRA:10019063]
Hallucinating [MedDRA:10019063]
Hallucination NOS [MedDRA:10019063]
Hallucinations [MedDRA:10019063]
Hallucinations aggravated [MedDRA:10019063]
Kinesthetic hallucination [MedDRA:10019063]
Organic hallucinosis syndrome [MedDRA:10019063]
Sensory hallucinations [MedDRA:10019063]
Stump hallucination [MedDRA:10019063]
Pseudohallucination [MedDRA:10019063]
Hallucinations (HCP) [OMIM:Hallucinations (HCP)]
Hallucinations (rare) [OMIM:Hallucinations (rare)]
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 [OMIM:Delirium]
Delirium (later-onset) [OMIM:Delirium (later-onset)]
Quality:
Cross references:
Orphanet:43590 "Delirium/hallucination" [Orphanet:43590]
OMIM: "Hallucination" [OMIM:Hallucination]
OMIM: "Hallucinations" [OMIM:Hallucinations]
OMIM: "Hallucinations (HCP)" [OMIM:Hallucinations (HCP)]
OMIM: "Hallucinations (rare)" [OMIM:Hallucinations (rare)]
OMIM: "Delirium" [OMIM:Delirium]
OMIM: "Delirium (later-onset)" [OMIM:Delirium (later-onset)]
UMLS:C0018524 "Hallucinations" [HPO:0000738]
UMLS:C0018524 "Hallucinations" [Orphanet:43590]
UMLS:C1285577 "Acute confusional state" [Orphanet:43590]
UMLS:C0011206 "Delirium" [Orphanet:43590]
Is a (Direct Parents):
Orphanet Behavioral abnormality
HPO         Behavioral abnormality
MedDRA Perception disturbances
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)
                Behavioral abnormality(HPO:0000708)
                   Hallucinations(HPO:0000738)
MedDRA:
Database Frequency: 60 / 7739
Resource:

All diseases associated with this symptom:

1q21.1 microduplication syndrome (Orphanet:250994)
4-hydroxybutyric aciduria (Orphanet:22)
Acro-oto-ocular syndrome (Orphanet:2980)
Acute intermittent porphyria (Orphanet:79276)
Alpha-mannosidosis (Orphanet:61)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Benign familial infantile seizures (Orphanet:306)
CLN1 disease (Orphanet:228329)
Cerebrotendinous xanthomatosis (Orphanet:909)
Classic maple syrup urine disease (Orphanet:268145)
Creutzfeldt-Jakob disease (Orphanet:204)
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 (OMIM:105550)
Frontotemporal dementia with motor neuron disease (Orphanet:275872)
Hartnup syndrome (Orphanet:2116)
Hereditary coproporphyria (Orphanet:79273)
Huntington disease (Orphanet:399)
Huntington disease-like 2 (Orphanet:98934)
Hypouricemia, renal, 2 (OMIM:612076)
Inherited Creutzfeldt-Jakob disease (Orphanet:282166)
Intermittent maple syrup urine disease (Orphanet:268173)
Isolated CoQ-cytochrome C reductase deficiency (Orphanet:1460)
Kufor-Rakeb syndrome (Orphanet:306674)
Legionellosis (Orphanet:549)
Lipoid proteinosis (Orphanet:530)
MELAS (Orphanet:550)
METACHROMATIC LEUKODYSTROPHY (OMIM:250100)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
NEUROPATHY, HEREDITARY SENSORY, TYPE IE (OMIM:614116)
Narcolepsy without cataplexy (Orphanet:83465)
Narcolepsy-cataplexy (Orphanet:2073)
Non-polyposis Turcot syndrome (Orphanet:99817)
Norrie disease (Orphanet:649)
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT (OMIM:605543)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
Perry syndrome (Orphanet:178509)
Porphyria (Orphanet:738)
Progressive non-fluent aphasia (Orphanet:100070)
Propionic acidemia (Orphanet:35)
Rabies (Orphanet:770)
Riboflavin transporter deficiency (Orphanet:97229)
Rift valley fever (Orphanet:319251)
SCHIZOPHRENIA (OMIM:181500)
SCHIZOPHRENIA 1 (OMIM:181510)
SCHIZOPHRENIA 10 (OMIM:605419)
Spinocerebellar ataxia type 17 (Orphanet:98759)
Thiamine-responsive maple syrup urine disease (Orphanet:268184)
Typhoid (Orphanet:99745)
Usher syndrome (Orphanet:886)
Usher syndrome type 1 (Orphanet:231169)
Usher syndrome type 2 (Orphanet:231178)
Usher syndrome type 3 (Orphanet:231183)
Wolfram syndrome (Orphanet:3463)
Wolfram-like syndrome (ORPHA:411590)
Woodhouse-Sakati syndrome (Orphanet:3464)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome (Orphanet:85295)
[DEL] Wolfram-like syndrome, autosomal dominant (OMIM:614296)