Psychosis

Symptom Information:

Symptom ID: HPO:0000709
Synonyms:
Psychotic disorder (disorder) [Orphanet:43630]
Psychotic symptom present (finding) [Orphanet:43630]
Psychotic [HPO:0000709]
Psychotic symptom present [Orphanet:43630]
Psychotic Disorders [Orphanet:43630]
Psychosis [OMIM:Psychosis]
Psychosis/schizophrenia/maniac disorder [Orphanet:43630]
Psychotic state [Orphanet:43630]
Psychotic disorder [Orphanet:43630]
Psychotic disorder [MedDRA:10061920]
Other nonorganic psychoses [MedDRA:10061920]
Paranoid psychosis [MedDRA:10061920]
Psychogenic paranoid psychosis [MedDRA:10061920]
Psychosis [MedDRA:10061920]
Psychosis NOS [MedDRA:10061920]
Psychosis paranoid [MedDRA:10061920]
Psychotic [MedDRA:10061920]
Psychotic disorder NOS [MedDRA:10061920]
Psychotic episode [MedDRA:10061920]
Psychotic reaction NOS [MedDRA:10061920]
Psychotic state [MedDRA:10061920]
Unspecified psychosis [MedDRA:10061920]
Psychosis aggravated [MedDRA:10061920]
Atypical psychosis [MedDRA:10061920]
Chronic psychosis [MedDRA:10061920]
Paranoid psychosis [OMIM:Paranoid psychosis]
Psychosis (1 patient) [OMIM:Psychosis (1 patient)]
Psychosis (25% of patients) [OMIM:Psychosis (25% of patients)]
Psychosis (if left untreated) [OMIM:Psychosis (if left untreated)]
Psychosis (in some patients) [OMIM:Psychosis (in some patients)]
Psychosis (rare) [OMIM:Psychosis (rare)]
Quality:
Cross references:
Orphanet:43630 "Psychosis/schizophrenia/maniac disorder" [Orphanet:43630]
OMIM: "Psychosis" [OMIM:Psychosis]
OMIM: "Paranoid psychosis" [OMIM:Paranoid psychosis]
OMIM: "Psychosis (1 patient)" [OMIM:Psychosis (1 patient)]
OMIM: "Psychosis (25% of patients)" [OMIM:Psychosis (25% of patients)]
OMIM: "Psychosis (if left untreated)" [OMIM:Psychosis (if left untreated)]
OMIM: "Psychosis (in some patients)" [OMIM:Psychosis (in some patients)]
OMIM: "Psychosis (rare)" [OMIM:Psychosis (rare)]
UMLS:C0033975 "Psychotic" [HPO:0000709]
UMLS:C0459435 "Psychotic symptom present" [Orphanet:43630]
UMLS:C0033975 "Psychotic Disorders" [Orphanet:43630]
Is a (Direct Parents):
MedDRA Psychotic disorder NEC
HPO         Behavioral abnormality
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)
                Behavioral abnormality(HPO:0000708)
                   Psychosis(HPO:0000709)
MedDRA:
Database Frequency: 61 / 7739
Resource:

All diseases associated with this symptom:

3q29 microdeletion syndrome (Orphanet:65286)
4-hydroxybutyric aciduria (Orphanet:22)
48,XXYY syndrome (Orphanet:10)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Adrenomyeloneuropathy (Orphanet:139399)
Alström syndrome (Orphanet:64)
Argininemia (Orphanet:90)
Argininosuccinic aciduria (Orphanet:23)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 (OMIM:615483)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
CADASIL (Orphanet:136)
CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY (OMIM:607674)
CLN3 disease (Orphanet:228346)
Cerebellar ataxia-deafness-narcolepsy syndrome (Orphanet:314404)
Choreoacanthocytosis (Orphanet:2388)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 (OMIM:615005)
Familial dementia, Danish type (Orphanet:97346)
Familial or sporadic hemiplegic migraine (Orphanet:569)
Female restricted epilepsy with intellectual deficit (Orphanet:101039)
Gerstmann-Straussler-Scheinker syndrome (Orphanet:356)
Hartnup syndrome (Orphanet:2116)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
LUJAN-FRYNS SYNDROME (OMIM:309520)
Lafora disease (Orphanet:501)
MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE (OMIM:248000)
MELAS (Orphanet:550)
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS (OMIM:613671)
MENTAL RETARDATION, X-LINKED 30 (OMIM:300558)
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 (OMIM:141500)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
Maternal hyperphenylalaninemia (Orphanet:2209)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
NIEMANN-PICK DISEASE, TYPE C1 (OMIM:257220)
NIEMANN-PICK DISEASE, TYPE C2 (OMIM:607625)
Norrie disease (Orphanet:649)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Phenylketonuria (Orphanet:716)
Porphyria variegata (Orphanet:79473)
Prader-Willi syndrome (Orphanet:739)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
SYSTEMIC LUPUS ERYTHEMATOSUS (OMIM:152700)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
WERNICKE-KORSAKOFF SYNDROME (OMIM:277730)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
Woodhouse-Sakati syndrome (Orphanet:3464)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)
X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome (Orphanet:85295)
[DEL] Wolfram-like syndrome, autosomal dominant (OMIM:614296)