Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Behavioral abnormality (HP:0000708)help
..Starting node
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Psychosis (HP:0000709)help
Term ID: 709
Name: Psychosis
Synonym: Psychosis
Definition: A condition characterized by changes of personality and thought patterns often accompanied by hallucinations and delusional beliefs.
Comments:
Reference: HP:0000709
Genes and Diseases:
 
       Child Nodes:
........expandPsychotic episodes (HP:0000725) help
................... HP:0006932 Transient psychotic episodes
........expandPsychotic mentation (HP:0001345) help

 Sister Nodes: 
..expandAbnormal consumption behavior (HP:0040202) help
..expandAbnormal emotion/affect behavior (HP:0100851) help
..expandAbnormal social behavior (HP:0012433) help
..expandAbnormal temper tantrums (HP:0025160) help
..expandAddictive behavior (HP:0030858) help
..expandAutistic behavior (HP:0000729) help
..expandDelusions (HP:0000746) help
..expandDrooling (HP:0002307) help
..expandEcholalia (HP:0010529) help
..expandHallucinations (HP:0000738) help
..expandHyperorality (HP:0000710) help
..expandImpairment in personality functioning (HP:0031466) help
..expandInflexible adherence to routines or rituals (HP:0000732) help
..expandLack of insight (HP:0000757) help
..expandLack of spontaneous play (HP:0000721) help
..expandLow frustration tolerance (HP:0000744) help
..expandMania (HP:0100754) help
..expandMutism (HP:0002300) help
..expandObsessive-compulsive behavior (HP:0000722) help
..expandobsolete Psychomotor retardation (HP:0025356) help
..expandOppositional defiant disorder (HP:0010865) help
..expandPerseveration (HP:0030223) help
..expandPersonality changes (HP:0000751) help
..expandPhotophobia (HP:0000613) help
..expandPseudobulbar behavioral symptoms (HP:0002193) help
..expandRestlessness (HP:0000711) help
..expandSchizophrenia (HP:0100753) help
..expandSelf-neglect (HP:0025479) help
..expandShort attention span (HP:0000736) help
..expandSleep disturbance (HP:0002360) help
..expandSound sensitivity (HP:0025112) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000709HP:0000709Psychosis0ABCD1 CL E G H21561OMIM:300100Adrenoleukodystrophy.135
HP:0000709HP:0000709Psychosis0ACADS CL E G H3590OMIM:201470Acyl-Coa dehydrogenase, short-chain, deficiency of.90
HP:0000709HP:0000709Psychosis0AIP CL E G H9049358OMIM:219090Pituitary adenoma 4, ACTH-secreting, somatic95
HP:0000709HP:0000709Psychosis0ALDH18A1 CL E G H58329722ORPHA:447753Autosomal dominant spastic paraplegia type 9AHP:0040283 - Occasional89
HP:0000709HP:0000709Psychosis0ALDH4A1 CL E G H8659406ORPHA:79101Hyperprolinemia type 274
HP:0000709HP:0000709Psychosis0ALDH5A1 CL E G H7915408OMIM:271980Succinic semialdehyde dehydrogenase deficiency.108
HP:0000709HP:0000709Psychosis0ARMC5 CL E G H7979825781ORPHA:189427Cushing syndrome due to macronodular adrenal hyperplasia7
HP:0000709HP:0000709Psychosis0ATP13A2 CL E G H2340030213OMIM:606693Kufor-Rakeb syndrome100
HP:0000709HP:0000709Psychosis0ATRX CL E G H546886ORPHA:96253Cushing diseaseHP:0040283 - Occasional169
HP:0000709HP:0000709Psychosis0ATXN7 CL E G H631410560ORPHA:94147Spinocerebellar ataxia type 7HP:0040283 - Occasional8
HP:0000709HP:0000709Psychosis0BRAF CL E G H6731097ORPHA:96253Cushing diseaseHP:0040283 - Occasional276
HP:0000709HP:0000709Psychosis0C9ORF72 CL E G H20322828337ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional56
HP:0000709HP:0000709Psychosis0C9ORF72 CL E G H20322828337ORPHA:401901Huntington disease-like syndrome due to C9ORF72 expansionsHP:0040283 - Occasional56
HP:0000709HP:0000709Psychosis0CABP4 CL E G H570101386ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy94
HP:0000709HP:0000709Psychosis0CACNA1A CL E G H7731388OMIM:141500Migraine, familial hemiplegic, 1.449
HP:0000709HP:0000709Psychosis0CBS CL E G H8751550ORPHA:394Classic homocystinuriaHP:0040283 - Occasional242
HP:0000709HP:0000709Psychosis0CDH23 CL E G H6407213733ORPHA:96253Cushing diseaseHP:0040283 - Occasional636
HP:0000709HP:0000709Psychosis0CHMP2B CL E G H2597824537ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional42
HP:0000709HP:0000709Psychosis0CHRNA2 CL E G H11351956ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy188
HP:0000709HP:0000709Psychosis0CHRNA4 CL E G H11371958ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy225
HP:0000709HP:0000709Psychosis0CHRNB2 CL E G H11411962ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy88
HP:0000709HP:0000709Psychosis0CLN3 CL E G H12012074OMIM:204200Ceroid lipofuscinosis, neuronal, 3.216
HP:0000709HP:0000709Psychosis0CLN3 CL E G H12012074ORPHA:228346CLN3 disease216
HP:0000709HP:0000709Psychosis0COX1 CL E G H45127419ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0COX2 CL E G H45137421ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0COX3 CL E G H45147422ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0CPOX CL E G H13712321ORPHA:79273Hereditary coproporphyriaHP:0040283 - Occasional72
HP:0000709HP:0000709Psychosis0CRH CL E G H13922355ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy1
HP:0000709HP:0000709Psychosis0CTLA4 CL E G H14932505OMIM:152700Systemic lupus erythematosus.10
HP:0000709HP:0000709Psychosis0DCAF17 CL E G H8006725784OMIM:241080Woodhouse-Sakati syndromeHP:0040283 - Occasional87
HP:0000709HP:0000709Psychosis0DCAF17 CL E G H8006725784ORPHA:3464Woodhouse-Sakati syndromeHP:0040283 - Occasional87
HP:0000709HP:0000709Psychosis0DEPDC5 CL E G H968118423ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy172
HP:0000709HP:0000709Psychosis0DNASE1 CL E G H17732956OMIM:152700Systemic lupus erythematosus.3
HP:0000709HP:0000709Psychosis0DNMT1 CL E G H17862976OMIM:604121Cerebellar ataxia, deafness, and narcolepsy, autosomal dominantHP:0040283 - Occasional145
HP:0000709HP:0000709Psychosis0EIF3F CL E G H86653275OMIM:618295Intellectual developmental disorder, autosomal recessive 67
HP:0000709HP:0000709Psychosis0EPM2A CL E G H79573413OMIM:254780Myoclonic epilepsy of lafora.83
HP:0000709HP:0000709Psychosis0FAR1 CL E G H8418826222ORPHA:447753Autosomal dominant spastic paraplegia type 9AHP:0040283 - Occasional7
HP:0000709HP:0000709Psychosis0FCGR2A CL E G H22123616OMIM:152700Systemic lupus erythematosus.6
HP:0000709HP:0000709Psychosis0FCGR2B CL E G H22133618OMIM:152700Systemic lupus erythematosus.2
HP:0000709HP:0000709Psychosis0FIG4 CL E G H989616873ORPHA:208441Bilateral parasagittal parieto-occipital polymicrogyria111
HP:0000709HP:0000709Psychosis0FRRS1L CL E G H237321362ORPHA:725Continuous spikes and waves during sleep4
HP:0000709HP:0000709Psychosis0FTL CL E G H25123999ORPHA:157846NeuroferritinopathyHP:0040284 - Very rare33
HP:0000709HP:0000709Psychosis0FUZ CL E G H8019926219ORPHA:1136Arnold-Chiari malformation type IIHP:0040284 - Very rare3
HP:0000709HP:0000709Psychosis0GCLC CL E G H27294311ORPHA:33574Glutamate-cysteine ligase deficiencyHP:0040283 - Occasional2
HP:0000709HP:0000709Psychosis0GNAS CL E G H27784392OMIM:219080ACTH-independent macronodular adrenal hyperplasia.101
HP:0000709HP:0000709Psychosis0GNAS CL E G H27784392ORPHA:189427Cushing syndrome due to macronodular adrenal hyperplasia101
HP:0000709HP:0000709Psychosis0GRIN2A CL E G H29034585ORPHA:725Continuous spikes and waves during sleep434
HP:0000709HP:0000709Psychosis0GRN CL E G H28964601ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional126
HP:0000709HP:0000709Psychosis0GSS CL E G H29374624OMIM:266130Glutathione synthetase deficiency39
HP:0000709HP:0000709Psychosis0H4C3 CL E G H83644787OMIM:619758TESSADORI-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 1; TEVANED1
HP:0000709HP:0000709Psychosis0HERC2 CL E G H89244868OMIM:176270Prader-Willi syndrome38
HP:0000709HP:0000709Psychosis0HFE CL E G H30774886OMIM:176200Porphyria variegata.38
HP:0000709HP:0000709Psychosis0HMBS CL E G H31454982OMIM:176000Porphyria, acute intermittent81
HP:0000709HP:0000709Psychosis0IPW CL E G H36536109OMIM:176270Prader-Willi syndrome
HP:0000709HP:0000709Psychosis0IRAK1 CL E G H36546112ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional
HP:0000709HP:0000709Psychosis0ITM2B CL E G H94456174OMIM:117300Dementia, familial danish.3
HP:0000709HP:0000709Psychosis0KCNN2 CL E G H37816291OMIM:619725NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE MOVEMENT OR BEHAVIORAL ABNORMALITIES; NEDMAB
HP:0000709HP:0000709Psychosis0KCNT1 CL E G H5758218865ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsy321
HP:0000709HP:0000709Psychosis0KCNT1 CL E G H5758218865OMIM:615005Epilepsy, nocturnal frontal lobe, 5HP:0040283 - Occasional321
HP:0000709HP:0000709Psychosis0MAGEL2 CL E G H545516814ORPHA:398069MAGEL2-related Prader-Willi-like syndromeHP:0040283 - Occasional63
HP:0000709HP:0000709Psychosis0MAGEL2 CL E G H545516814OMIM:176270Prader-Willi syndrome63
HP:0000709HP:0000709Psychosis0MAGEL2 CL E G H545516814ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040282 - Frequent63
HP:0000709HP:0000709Psychosis0MAGEL2 CL E G H545516814ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040282 - Frequent63
HP:0000709HP:0000709Psychosis0MAGEL2 CL E G H545516814ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040282 - Frequent63
HP:0000709HP:0000709Psychosis0MAPT CL E G H41376893ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional140
HP:0000709HP:0000709Psychosis0MECP2 CL E G H42046990OMIM:300055Mental retardation, X-linked, syndromic 13950
HP:0000709HP:0000709Psychosis0MED12 CL E G H996811957ORPHA:776Lujan-Fryns syndromeHP:0040283 - Occasional228
HP:0000709HP:0000709Psychosis0MED12 CL E G H996811957OMIM:309520Lujan-Fryns syndrome.228
HP:0000709HP:0000709Psychosis0MKRN3 CL E G H76817114OMIM:176270Prader-Willi syndrome5
HP:0000709HP:0000709Psychosis0MKRN3-AS1 CL E G H10108OMIM:176270Prader-Willi syndrome
HP:0000709HP:0000709Psychosis0MMACHC CL E G H2597424525ORPHA:79282Methylmalonic acidemia with homocystinuria, type cblCHP:0040284 - Very rare101
HP:0000709HP:0000709Psychosis0MTHFR CL E G H45247436ORPHA:395Homocystinuria due to methylene tetrahydrofolate reductase deficiencyHP:0040283 - Occasional183
HP:0000709HP:0000709Psychosis0MYORG CL E G H5746219918OMIM:618317Basal ganglia calcification, idiopathic, 7, autosomal recessiveHP:0040284 - Very rare
HP:0000709HP:0000709Psychosis0NAGS CL E G H16241717996ORPHA:927Hyperammonemia due to N-acetylglutamate synthase deficiency36
HP:0000709HP:0000709Psychosis0ND1 CL E G H45357455ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0ND4 CL E G H45387459ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0ND5 CL E G H45407461ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0ND6 CL E G H45417462ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0NDN CL E G H46927675ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0NDN CL E G H46927675ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0NDN CL E G H46927675ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0NDP CL E G H46937678ORPHA:649Norrie diseaseHP:0040282 - Frequent39
HP:0000709HP:0000709Psychosis0NDP CL E G H46937678OMIM:310600Norrie disease.39
HP:0000709HP:0000709Psychosis0NHLRC1 CL E G H37888421576OMIM:254780Myoclonic epilepsy of lafora.77
HP:0000709HP:0000709Psychosis0NOTCH3 CL E G H48547883OMIM:125310Cerebral arteriopathy, autosomal dominant, with subcortical infarctsand leukoencephalopathy144
HP:0000709HP:0000709Psychosis0NPAP1 CL E G H237421190OMIM:176270Prader-Willi syndrome1
HP:0000709HP:0000709Psychosis0NPC1 CL E G H48647897OMIM:257220Niemann-pick disease, type C1.258
HP:0000709HP:0000709Psychosis0NPC2 CL E G H1057714537OMIM:607625Niemann-pick disease, type C2.33
HP:0000709HP:0000709Psychosis0NR3C1 CL E G H29087978ORPHA:96253Cushing diseaseHP:0040283 - Occasional79
HP:0000709HP:0000709Psychosis0OCA2 CL E G H49488101ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040282 - Frequent121
HP:0000709HP:0000709Psychosis0OCA2 CL E G H49488101ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040282 - Frequent121
HP:0000709HP:0000709Psychosis0OCA2 CL E G H49488101ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040282 - Frequent121
HP:0000709HP:0000709Psychosis0PAK3 CL E G H50638592OMIM:300558MENTAL RETARDATION, X-LINKED 30; MRX3027
HP:0000709HP:0000709Psychosis0PANK2 CL E G H8002515894ORPHA:216873Atypical pantothenate kinase-associated neurodegenerationHP:0040284 - Very rare55
HP:0000709HP:0000709Psychosis0PARK7 CL E G H1131516369OMIM:606324PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET; PARK723
HP:0000709HP:0000709Psychosis0PCDH19 CL E G H5752614270OMIM:300088Epileptic encephalopathy, early infantile, 9.225
HP:0000709HP:0000709Psychosis0PCDH19 CL E G H5752614270ORPHA:101039Female restricted epilepsy with intellectual disabilityHP:0040284 - Very rare225
HP:0000709HP:0000709Psychosis0PDE11A CL E G H509408773OMIM:610475Pigmented nodular adrenocortical disease, primary, 2.13
HP:0000709HP:0000709Psychosis0PDE11A CL E G H509408773ORPHA:189439Primary pigmented nodular adrenocortical disease13
HP:0000709HP:0000709Psychosis0PDE8B CL E G H86228794ORPHA:189439Primary pigmented nodular adrenocortical disease75
HP:0000709HP:0000709Psychosis0PDGFB CL E G H51558800OMIM:213600Basal ganglia calcification, idiopathic, 1.9
HP:0000709HP:0000709Psychosis0PDGFB CL E G H51558800OMIM:615483Basal ganglia calcification, idiopathic, 5.9
HP:0000709HP:0000709Psychosis0PDGFRB CL E G H51598804OMIM:213600Basal ganglia calcification, idiopathic, 1.28
HP:0000709HP:0000709Psychosis0PIDD1 CL E G H5536716491OMIM:619827INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 75, WITH NEUROPSYCHIATRIC FEATURES AND VARIANT LISSENCEPHALY; MRT75
HP:0000709HP:0000709Psychosis0PITRM1 CL E G H1053117663OMIM:619405SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 30; SCAR301
HP:0000709HP:0000709Psychosis0PPOX CL E G H54989280OMIM:176200Porphyria variegata.41
HP:0000709HP:0000709Psychosis0PRDM8 CL E G H5697813993OMIM:616640Epilepsy, progressive myoclonic, 10.1
HP:0000709HP:0000709Psychosis0PRKACA CL E G H55669380ORPHA:189439Primary pigmented nodular adrenocortical disease2
HP:0000709HP:0000709Psychosis0PRKAR1A CL E G H55739388OMIM:610489Pigmented nodular adrenocortical disease, primary, 1.134
HP:0000709HP:0000709Psychosis0PRKAR1A CL E G H55739388ORPHA:189439Primary pigmented nodular adrenocortical disease134
HP:0000709HP:0000709Psychosis0PRNP CL E G H56219449OMIM:137440Gerstmann-Straussler disease.69
HP:0000709HP:0000709Psychosis0PRORP CL E G H969219958OMIM:619737COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 54; COXPD54
HP:0000709HP:0000709Psychosis0PSEN1 CL E G H56639508ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional241
HP:0000709HP:0000709Psychosis0PTPN22 CL E G H261919652OMIM:152700Systemic lupus erythematosus.3
HP:0000709HP:0000709Psychosis0PUS3 CL E G H8348025461ORPHA:488627Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndromeHP:0040283 - Occasional1
HP:0000709HP:0000709Psychosis0PWAR1 CL E G H14562430089OMIM:176270Prader-Willi syndrome
HP:0000709HP:0000709Psychosis0PWRN1 CL E G H79111433235OMIM:176270Prader-Willi syndrome
HP:0000709HP:0000709Psychosis0RPS6KA3 CL E G H619710432ORPHA:276630Symptomatic form of Coffin-Lowry syndrome in female carriersHP:0040283 - Occasional65
HP:0000709HP:0000709Psychosis0SIM1 CL E G H649210882ORPHA:398079SIM1-related Prader-Willi-like syndromeHP:0040283 - Occasional40
HP:0000709HP:0000709Psychosis0SLC12A6 CL E G H999010914OMIM:218000Agenesis of the corpus callosum with peripheral neuropathy.163
HP:0000709HP:0000709Psychosis0SLC20A2 CL E G H657510947OMIM:213600Basal ganglia calcification, idiopathic, 1.70
HP:0000709HP:0000709Psychosis0SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type IIHP:0040283 - Occasional82
HP:0000709HP:0000709Psychosis0SLC6A19 CL E G H34002427960OMIM:234500Hartnup disorder.12
HP:0000709HP:0000709Psychosis0SLC7A7 CL E G H905611065OMIM:222700Lysinuric protein intolerance104
HP:0000709HP:0000709Psychosis0SNORD115-1 CL E G H33843333020OMIM:176270Prader-Willi syndrome
HP:0000709HP:0000709Psychosis0SNORD116-1 CL E G H10003341333067OMIM:176270Prader-Willi syndrome
HP:0000709HP:0000709Psychosis0SNORD118 CL E G H72767632952ORPHA:542310Leukoencephalopathy with calcifications and cysts6
HP:0000709HP:0000709Psychosis0SNRPN CL E G H663811164ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040282 - Frequent37
HP:0000709HP:0000709Psychosis0SNRPN CL E G H663811164ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040282 - Frequent37
HP:0000709HP:0000709Psychosis0SNRPN CL E G H663811164ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040282 - Frequent37
HP:0000709HP:0000709Psychosis0SOBP CL E G H5508429256OMIM:613671Mental retardation, anterior maxillary protrusion, and strabismusHP:0040283 - Occasional29
HP:0000709HP:0000709Psychosis0SPART CL E G H2311118514ORPHA:101000Autosomal recessive spastic paraplegia type 20HP:0040283 - Occasional66
HP:0000709HP:0000709Psychosis0SPG11 CL E G H8020811226ORPHA:2822Autosomal recessive spastic paraplegia type 11HP:0040283 - Occasional287
HP:0000709HP:0000709Psychosis0SPP1 CL E G H669611255ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional
HP:0000709HP:0000709Psychosis0SQSTM1 CL E G H887811280ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional62
HP:0000709HP:0000709Psychosis0SRCAP CL E G H1084716974OMIM:619595DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA138
HP:0000709HP:0000709Psychosis0STAT4 CL E G H677511365ORPHA:93552Pediatric systemic lupus erythematosusHP:0040283 - Occasional2
HP:0000709HP:0000709Psychosis0TBC1D7 CL E G H5125621066OMIM:248000Macrocephaly/megalencephaly syndrome, autosomal recessiveHP:0040283 - Occasional4
HP:0000709HP:0000709Psychosis0TMEM106B CL E G H5466422407ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional
HP:0000709HP:0000709Psychosis0TMEM106B CL E G H5466422407OMIM:617964Leukodystrophy, hypomyelinating, 16
HP:0000709HP:0000709Psychosis0TP53 CL E G H715711998ORPHA:96253Cushing diseaseHP:0040283 - Occasional911
HP:0000709HP:0000709Psychosis0TREM2 CL E G H5420917761ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional31
HP:0000709HP:0000709Psychosis0TREX1 CL E G H1127712269ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsHP:0040283 - Occasional56
HP:0000709HP:0000709Psychosis0TREX1 CL E G H1127712269OMIM:152700Systemic lupus erythematosus.56
HP:0000709HP:0000709Psychosis0TRNF CL E G H45587481ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0TRNH CL E G H45647487ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0TRNL1 CL E G H45677490ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0TRNQ CL E G H45727495ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0TRNS1 CL E G H45747497ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0TRNS2 CL E G H45757498ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0TRNW CL E G H45787501ORPHA:550MELASHP:0040282 - Frequent
HP:0000709HP:0000709Psychosis0TRRAP CL E G H829512347OMIM:618454Developmental delay with or without dysmorphic facies and autism2
HP:0000709HP:0000709Psychosis0TTC19 CL E G H5490226006OMIM:615157Mitochondrial complex III deficiency, nuclear type 2.88
HP:0000709HP:0000709Psychosis0TWNK CL E G H566521160OMIM:271245Mitochondrial DNA depletion syndrome 7 (hepatocerebral type).113
HP:0000709HP:0000709Psychosis0UPF3B CL E G H6510920439ORPHA:776Lujan-Fryns syndromeHP:0040283 - Occasional33
HP:0000709HP:0000709Psychosis0USP48 CL E G H8419618533ORPHA:96253Cushing diseaseHP:0040283 - Occasional1
HP:0000709HP:0000709Psychosis0USP8 CL E G H910112631ORPHA:96253Cushing diseaseHP:0040283 - Occasional7
HP:0000709HP:0000709Psychosis0USP8 CL E G H910112631OMIM:219090Pituitary adenoma 4, ACTH-secreting, somatic7
HP:0000709HP:0000709Psychosis0VCP CL E G H741512666ORPHA:275864Behavioral variant of frontotemporal dementiaHP:0040283 - Occasional63
HP:0000709HP:0000709Psychosis0VPS13A CL E G H232301908OMIM:200150CHOREOACANTHOCYTOSIS.130
HP:0000709HP:0000709Psychosis0WARS2 CL E G H1035212730OMIM:619738PARKINSONISM-DYSTONIA 3, CHILDHOOD-ONSET; PKDYS32
HP:0000709HP:0000709Psychosis0WFS1 CL E G H746612762ORPHA:411590Wolfram-like syndromeHP:0040281 - Very frequent389
HP:0000709HP:0000709Psychosis0ZDHHC9 CL E G H5111418475ORPHA:776Lujan-Fryns syndromeHP:0040283 - Occasional10
HP:0000709HP:0000709Psychosis0ZFYVE26 CL E G H2350320761OMIM:270700Spastic paraplegia 15, autosomal recessive.189
HP:0000709HP:0000709Psychosis0ZMYM2 CL E G H775012989OMIM:619522NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES; NECRC
HP:0000709HP:0001345Psychotic mentation1AIP CL E G H9049358OMIM:219090Pituitary adenoma 4, ACTH-secreting, somatic.95
HP:0000709HP:0001345Psychotic mentation1ALDH4A1 CL E G H8659406ORPHA:79101Hyperprolinemia type 2HP:0040283 - Occasional74
HP:0000709HP:0000725Psychotic episodes1ARMC5 CL E G H7979825781ORPHA:189427Cushing syndrome due to macronodular adrenal hyperplasia7
HP:0000709HP:0000725Psychotic episodes1ATP13A2 CL E G H2340030213OMIM:606693Kufor-Rakeb syndrome.100
HP:0000709HP:0000725Psychotic episodes1ATRX CL E G H546886ORPHA:96253Cushing disease169
HP:0000709HP:0000725Psychotic episodes1BRAF CL E G H6731097ORPHA:96253Cushing disease276
HP:0000709HP:0001345Psychotic mentation1CABP4 CL E G H570101386ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare94
HP:0000709HP:0000725Psychotic episodes1CDH23 CL E G H6407213733ORPHA:96253Cushing disease636
HP:0000709HP:0001345Psychotic mentation1CHRNA2 CL E G H11351956ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare188
HP:0000709HP:0001345Psychotic mentation1CHRNA4 CL E G H11371958ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare225
HP:0000709HP:0001345Psychotic mentation1CHRNB2 CL E G H11411962ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare88
HP:0000709HP:0001345Psychotic mentation1COX1 CL E G H45127419ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1COX2 CL E G H45137421ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1COX3 CL E G H45147422ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1CRH CL E G H13922355ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare1
HP:0000709HP:0001345Psychotic mentation1DEPDC5 CL E G H968118423ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare172
HP:0000709HP:0001345Psychotic mentation1FIG4 CL E G H989616873ORPHA:208441Bilateral parasagittal parieto-occipital polymicrogyriaHP:0040283 - Occasional111
HP:0000709HP:0001345Psychotic mentation1FRRS1L CL E G H237321362ORPHA:725Continuous spikes and waves during sleepHP:0040283 - Occasional4
HP:0000709HP:0000725Psychotic episodes1GNAS CL E G H27784392ORPHA:189427Cushing syndrome due to macronodular adrenal hyperplasia101
HP:0000709HP:0001345Psychotic mentation1GRIN2A CL E G H29034585ORPHA:725Continuous spikes and waves during sleepHP:0040283 - Occasional434
HP:0000709HP:0001345Psychotic mentation1GSS CL E G H29374624OMIM:266130Glutathione synthetase deficiency.39
HP:0000709HP:0000725Psychotic episodes1HMBS CL E G H31454982OMIM:176000Porphyria, acute intermittent.81
HP:0000709HP:0001345Psychotic mentation1KCNT1 CL E G H5758218865ORPHA:98784Autosomal dominant nocturnal frontal lobe epilepsyHP:0040284 - Very rare321
HP:0000709HP:0001345Psychotic mentation1MTHFR CL E G H45247436ORPHA:395Homocystinuria due to methylene tetrahydrofolate reductase deficiencyHP:0040283 - Occasional183
HP:0000709HP:0000725Psychotic episodes1MTHFR CL E G H45247436ORPHA:395Homocystinuria due to methylene tetrahydrofolate reductase deficiencyHP:0040282 - Frequent183
HP:0000709HP:0000725Psychotic episodes1NAGS CL E G H16241717996ORPHA:927Hyperammonemia due to N-acetylglutamate synthase deficiencyHP:0040284 - Very rare36
HP:0000709HP:0001345Psychotic mentation1ND1 CL E G H45357455ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1ND4 CL E G H45387459ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1ND5 CL E G H45407461ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1ND6 CL E G H45417462ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0000725Psychotic episodes1NR3C1 CL E G H29087978ORPHA:96253Cushing disease79
HP:0000709HP:0000725Psychotic episodes1PARK7 CL E G H1131516369OMIM:606324PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET; PARK723
HP:0000709HP:0000725Psychotic episodes1PDE11A CL E G H509408773ORPHA:189439Primary pigmented nodular adrenocortical disease13
HP:0000709HP:0000725Psychotic episodes1PDE8B CL E G H86228794ORPHA:189439Primary pigmented nodular adrenocortical disease75
HP:0000709HP:0000725Psychotic episodes1PITRM1 CL E G H1053117663OMIM:619405SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 30; SCAR301
HP:0000709HP:0000725Psychotic episodes1PRKACA CL E G H55669380ORPHA:189439Primary pigmented nodular adrenocortical disease2
HP:0000709HP:0000725Psychotic episodes1PRKAR1A CL E G H55739388ORPHA:189439Primary pigmented nodular adrenocortical disease134
HP:0000709HP:0000725Psychotic episodes1SLC7A7 CL E G H905611065OMIM:222700Lysinuric protein intoleranceHP:0040283 - Occasional104
HP:0000709HP:0000725Psychotic episodes1SNORD118 CL E G H72767632952ORPHA:542310Leukoencephalopathy with calcifications and cysts6
HP:0000709HP:0000725Psychotic episodes1TP53 CL E G H715711998ORPHA:96253Cushing disease911
HP:0000709HP:0001345Psychotic mentation1TRNF CL E G H45587481ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1TRNH CL E G H45647487ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1TRNL1 CL E G H45677490ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1TRNQ CL E G H45727495ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1TRNS1 CL E G H45747497ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1TRNS2 CL E G H45757498ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0001345Psychotic mentation1TRNW CL E G H45787501ORPHA:550MELASHP:0040283 - Occasional
HP:0000709HP:0000725Psychotic episodes1USP48 CL E G H8419618533ORPHA:96253Cushing disease1
HP:0000709HP:0000725Psychotic episodes1USP8 CL E G H910112631ORPHA:96253Cushing disease7
HP:0000709HP:0001345Psychotic mentation1USP8 CL E G H910112631OMIM:219090Pituitary adenoma 4, ACTH-secreting, somatic.7
HP:0000709HP:0006932Transient psychotic episodes2 CL E G H


Genes (141) :ABCD1 ACADS AIP ALDH18A1 ALDH4A1 ALDH5A1 ARMC5 ATP13A2 ATRX ATXN7 BRAF C9ORF72 CABP4 CACNA1A CBS CDH23 CHMP2B CHRNA2 CHRNA4 CHRNB2 CLN3 COX1 COX2 COX3 CPOX CRH CTLA4 DCAF17 DEPDC5 DNASE1 DNMT1 EIF3F EPM2A FAR1 FCGR2A FCGR2B FIG4 FRRS1L FTL FUZ GCLC GNAS GRIN2A GRN GSS H4C3 HERC2 HFE HMBS IPW IRAK1 ITM2B KCNN2 KCNT1 MAGEL2 MAPT MECP2 MED12 MKRN3 MKRN3-AS1 MMACHC MTHFR MYORG NAGS ND1 ND4 ND5 ND6 NDN NDP NHLRC1 NOTCH3 NPAP1 NPC1 NPC2 NR3C1 OCA2 PAK3 PANK2 PARK7 PCDH19 PDE11A PDE8B PDGFB PDGFRB PIDD1 PITRM1 PPOX PRDM8 PRKACA PRKAR1A PRNP PRORP PSEN1 PTPN22 PUS3 PWAR1 PWRN1 RPS6KA3 SIM1 SLC12A6 SLC20A2 SLC25A13 SLC6A19 SLC7A7 SNORD115-1 SNORD116-1 SNORD118 SNRPN SOBP SPART SPG11 SPP1 SQSTM1 SRCAP STAT4 TBC1D7 TMEM106B TP53 TREM2 TREX1 TRNF TRNH TRNL1 TRNQ TRNS1 TRNS2 TRNW TRRAP TTC19 TWNK UPF3B USP48 USP8 VCP VPS13A WARS2 WFS1 ZDHHC9 ZFYVE26 ZMYM2

Diseases (94) :OMIM:300100 OMIM:201470 OMIM:219090 ORPHA:447753 ORPHA:79101 OMIM:271980 ORPHA:189427 OMIM:606693 ORPHA:96253 ORPHA:94147 ORPHA:275864 ORPHA:401901 ORPHA:98784 OMIM:141500 ORPHA:394 OMIM:204200 ORPHA:228346 ORPHA:550 ORPHA:79273 OMIM:152700 OMIM:241080 ORPHA:3464 OMIM:604121 OMIM:618295 OMIM:254780 ORPHA:208441 ORPHA:725 ORPHA:157846 ORPHA:1136 ORPHA:33574 OMIM:219080 OMIM:266130 OMIM:619758 OMIM:176270 OMIM:176200 OMIM:176000 ORPHA:93552 OMIM:117300 OMIM:619725 OMIM:615005 ORPHA:398069 ORPHA:98754 ORPHA:177901 ORPHA:177904 OMIM:300055 ORPHA:776 OMIM:309520 ORPHA:79282 ORPHA:395 OMIM:618317 ORPHA:927 ORPHA:649 OMIM:310600 OMIM:125310 OMIM:257220 OMIM:607625 OMIM:300558 ORPHA:216873 OMIM:606324 OMIM:300088 ORPHA:101039 OMIM:610475 ORPHA:189439 OMIM:213600 OMIM:615483 OMIM:619827 OMIM:619405 OMIM:616640 OMIM:610489 OMIM:137440 OMIM:619737 ORPHA:488627 ORPHA:276630 ORPHA:398079 OMIM:218000 ORPHA:247585 OMIM:234500 OMIM:222700 ORPHA:542310 OMIM:613671 ORPHA:101000 ORPHA:2822 OMIM:619595 OMIM:248000 OMIM:617964 ORPHA:247691 OMIM:618454 OMIM:615157 OMIM:271245 OMIM:200150 OMIM:619738 ORPHA:411590 OMIM:270700 OMIM:619522
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.