Psychosis
Symptom Information:
Symptom ID: | HPO:0000709 | |||||||||||||||||||||||||||||||
Synonyms: |
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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) Behavioral abnormality(HPO:0000708) Psychosis(HPO:0000709) MedDRA: |
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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) |