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
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Hallucinations (HP:0000738)help
Term ID: 738
Name: Hallucinations
Synonym: Hallucination; Hallucinations; Sensory hallucination
Definition: Perceptions in a conscious and awake state in the absence of external stimuli which have qualities of real perception, in that they are vivid, substantial, and located in external objective space.
Comments:
Reference: HP:0000738
Genes and Diseases:
 
       Child Nodes:
........expandVisual hallucinations (HP:0002367) help
........expandHypnagogic hallucinations (HP:0002519) help
........expandVivid hallucinations (HP:0006803) help
........expandHypnopompic hallucinations (HP:0006896) help
........expandAuditory hallucinations (HP:0008765) 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
..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
..expandPsychosis (HP:0000709) 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:0000738HP:0000738Hallucinations0ABCA7 CL E G H1034737ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040281 - Very frequent3
HP:0000738HP:0000738Hallucinations0ADGRV1 CL E G H8405917416ORPHA:231178Usher syndrome type 2HP:0040283 - Occasional530
HP:0000738HP:0000738Hallucinations0ADH1C CL E G H126251OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional4
HP:0000738HP:0000738Hallucinations0ALAD CL E G H210395ORPHA:100924Porphyria due to ALA dehydratase deficiencyHP:0040283 - Occasional62
HP:0000738HP:0000738Hallucinations0ALDH4A1 CL E G H8659406ORPHA:79101Hyperprolinemia type 2HP:0040283 - Occasional74
HP:0000738HP:0000738Hallucinations0ALDH5A1 CL E G H7915408OMIM:271980Succinic semialdehyde dehydrogenase deficiency.108
HP:0000738HP:0000738Hallucinations0APOL2 CL E G H23780619OMIM:181500SCHIZOPHRENIA.
HP:0000738HP:0000738Hallucinations0APOL4 CL E G H8083214867OMIM:181500SCHIZOPHRENIA.
HP:0000738HP:0000738Hallucinations0APP CL E G H351620ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040281 - Very frequent74
HP:0000738HP:0000738Hallucinations0ARSA CL E G H410713OMIM:250100Metachromatic leukodystrophy.253
HP:0000738HP:0000738Hallucinations0ARSA CL E G H410713ORPHA:309271Metachromatic leukodystrophy, adult formHP:0040282 - Frequent253
HP:0000738HP:0000738Hallucinations0ARSA CL E G H410713ORPHA:309263Metachromatic leukodystrophy, juvenile formHP:0040283 - Occasional253
HP:0000738HP:0000738Hallucinations0ARSA CL E G H410713ORPHA:309256Metachromatic leukodystrophy, late infantile formHP:0040283 - Occasional253
HP:0000738HP:0000738Hallucinations0ARSG CL E G H2290124102ORPHA:231183Usher syndrome type 3HP:0040283 - Occasional
HP:0000738HP:0000738Hallucinations0ATP13A2 CL E G H2340030213ORPHA:513436Autosomal recessive spastic paraplegia type 78HP:0040284 - Very rare100
HP:0000738HP:0000738Hallucinations0ATP13A2 CL E G H2340030213ORPHA:306674Kufor-Rakeb syndrome100
HP:0000738HP:0000738Hallucinations0ATP13A2 CL E G H2340030213OMIM:606693Kufor-Rakeb syndrome100
HP:0000738HP:0000738Hallucinations0ATP13A2 CL E G H2340030213OMIM:617225SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE; SPG78100
HP:0000738HP:0000738Hallucinations0ATXN2 CL E G H631110555OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional11
HP:0000738HP:0000738Hallucinations0ATXN8OS CL E G H631510561OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional1
HP:0000738HP:0000738Hallucinations0BCKDHA CL E G H593986OMIM:248600Maple syrup urine disease.120
HP:0000738HP:0000738Hallucinations0BCKDHB CL E G H594987OMIM:248600Maple syrup urine disease.162
HP:0000738HP:0000738Hallucinations0BCS1L CL E G H6171020OMIM:124000Mitochondrial complex III deficiency, nuclear type 1.72
HP:0000738HP:0000738Hallucinations0BMPR1A CL E G H6571076ORPHA:440437Familial colorectal cancer Type XHP:0040283 - Occasional385
HP:0000738HP:0000738Hallucinations0BPTF CL E G H21863581ORPHA:52996217q24.2 microdeletion syndromeHP:0040283 - Occasional2
HP:0000738HP:0000738Hallucinations0C9ORF72 CL E G H20322828337OMIM:105550Amyotrophic lateral sclerosis and/or frontotemporal dementia 1.56
HP:0000738HP:0000738Hallucinations0C9ORF72 CL E G H20322828337ORPHA:275872Frontotemporal dementia with motor neuron diseaseHP:0040282 - Frequent56
HP:0000738HP:0000738Hallucinations0CACNA1A CL E G H7731388OMIM:141500Migraine, familial hemiplegic, 1449
HP:0000738HP:0000738Hallucinations0CDH2 CL E G H10001759OMIM:618929AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS
HP:0000738HP:0000738Hallucinations0CDH23 CL E G H6407213733ORPHA:231169Usher syndrome type 1HP:0040283 - Occasional636
HP:0000738HP:0000738Hallucinations0CEP78 CL E G H8413125740ORPHA:231183Usher syndrome type 3HP:0040283 - Occasional9
HP:0000738HP:0000738Hallucinations0CEP85L CL E G H38711921638OMIM:618873LISSENCEPHALY 10; LIS101
HP:0000738HP:0000738Hallucinations0CHCHD10 CL E G H40091615559ORPHA:275872Frontotemporal dementia with motor neuron diseaseHP:0040282 - Frequent11
HP:0000738HP:0000738Hallucinations0CHI3L1 CL E G H11161932OMIM:181500SCHIZOPHRENIA.1
HP:0000738HP:0000738Hallucinations0CIB2 CL E G H1051824579ORPHA:231169Usher syndrome type 1HP:0040283 - Occasional15
HP:0000738HP:0000738Hallucinations0CISD2 CL E G H49385624212ORPHA:3463Wolfram syndromeHP:0040283 - Occasional3
HP:0000738HP:0000738Hallucinations0CLN3 CL E G H12012074ORPHA:228346CLN3 disease216
HP:0000738HP:0000738Hallucinations0CLN5 CL E G H12032076ORPHA:228360CLN5 diseaseHP:0040283 - Occasional141
HP:0000738HP:0000738Hallucinations0CLN6 CL E G H549822077OMIM:204300Ceroid lipofuscinosis, neuronal, 4A, autosomal recessive143
HP:0000738HP:0000738Hallucinations0CLRN1 CL E G H740112605ORPHA:231183Usher syndrome type 3HP:0040283 - Occasional60
HP:0000738HP:0000738Hallucinations0CLTRN CL E G H5739329437ORPHA:2116Hartnup diseaseHP:0040281 - Very frequent
HP:0000738HP:0000738Hallucinations0COMT CL E G H13122228OMIM:181500SCHIZOPHRENIA.6
HP:0000738HP:0000738Hallucinations0CPOX CL E G H13712321OMIM:121300Coproporphyria.72
HP:0000738HP:0000738Hallucinations0CSF1R CL E G H14362433OMIM:221820Leukoencephalopathy, diffuse hereditary, with spheroids149
HP:0000738HP:0000738Hallucinations0CTSH CL E G H15122535ORPHA:2073Narcolepsy type 1HP:0040281 - Very frequent1
HP:0000738HP:0000738Hallucinations0CYP27A1 CL E G H15932605ORPHA:909Cerebrotendinous xanthomatosisHP:0040283 - Occasional114
HP:0000738HP:0000738Hallucinations0CYP27A1 CL E G H15932605OMIM:213700Cerebrotendinous xanthomatosis.114
HP:0000738HP:0000738Hallucinations0DAOA CL E G H26701221191OMIM:181500SCHIZOPHRENIA.
HP:0000738HP:0000738Hallucinations0DBT CL E G H16292698OMIM:248600Maple syrup urine disease.156
HP:0000738HP:0000738Hallucinations0DCAF17 CL E G H8006725784ORPHA:3464Woodhouse-Sakati syndromeHP:0040283 - Occasional87
HP:0000738HP:0000738Hallucinations0DCAF17 CL E G H8006725784OMIM:241080Woodhouse-Sakati syndromeHP:0040283 - Occasional87
HP:0000738HP:0000738Hallucinations0DEPDC5 CL E G H968118423ORPHA:101046Autosomal dominant epilepsy with auditory features172
HP:0000738HP:0000738Hallucinations0DEPDC5 CL E G H968118423ORPHA:98820Familial focal epilepsy with variable foci172
HP:0000738HP:0000738Hallucinations0DISC2 CL E G H271842889OMIM:181500SCHIZOPHRENIA.
HP:0000738HP:0000738Hallucinations0DNAJC13 CL E G H2331730343ORPHA:411602Hereditary late-onset Parkinson disease2
HP:0000738HP:0000738Hallucinations0DNAJC5 CL E G H8033116235OMIM:162350Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant155
HP:0000738HP:0000738Hallucinations0DNAJC6 CL E G H982915469OMIM:615528Parkinson disease 19a, juvenile-onset.6
HP:0000738HP:0000738Hallucinations0DNAJC6 CL E G H982915469ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent6
HP:0000738HP:0000738Hallucinations0DNM1L CL E G H100592973ORPHA:98673Autosomal dominant optic atrophy, classic formHP:0040284 - Very rare94
HP:0000738HP:0000738Hallucinations0DRD3 CL E G H18143024OMIM:181500SCHIZOPHRENIA.21
HP:0000738HP:0000738Hallucinations0ECM1 CL E G H18933153OMIM:247100Urbach-Wiethe disease.14
HP:0000738HP:0000738Hallucinations0EIF4G1 CL E G H19813296ORPHA:411602Hereditary late-onset Parkinson disease2
HP:0000738HP:0000738Hallucinations0EPCAM CL E G H407211529ORPHA:144Lynch syndromeHP:0040283 - Occasional170
HP:0000738HP:0000738Hallucinations0EPM2A CL E G H79573413ORPHA:501Lafora disease83
HP:0000738HP:0000738Hallucinations0EPM2A CL E G H79573413OMIM:254780Myoclonic epilepsy of lafora83
HP:0000738HP:0000738Hallucinations0ESPN CL E G H8371513281ORPHA:231169Usher syndrome type 1HP:0040283 - Occasional33
HP:0000738HP:0000738Hallucinations0FAN1 CL E G H2290929170ORPHA:144Lynch syndromeHP:0040283 - Occasional15
HP:0000738HP:0000738Hallucinations0FBXO7 CL E G H2579313586ORPHA:171695Parkinsonian-pyramidal syndrome36
HP:0000738HP:0000738Hallucinations0FIG4 CL E G H989616873ORPHA:208441Bilateral parasagittal parieto-occipital polymicrogyria111
HP:0000738HP:0000738Hallucinations0FIG4 CL E G H989616873OMIM:612691Polymicrogyria, bilateral temporooccipital111
HP:0000738HP:0000738Hallucinations0FUS CL E G H25214010ORPHA:275872Frontotemporal dementia with motor neuron diseaseHP:0040282 - Frequent105
HP:0000738HP:0000738Hallucinations0GBA1 CL E G H26294177OMIM:127750Dementia, lewy body
HP:0000738HP:0000738Hallucinations0GBA1 CL E G H26294177ORPHA:411602Hereditary late-onset Parkinson disease
HP:0000738HP:0000738Hallucinations0GBA1 CL E G H26294177OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional
HP:0000738HP:0000738Hallucinations0GIGYF2 CL E G H2605811960ORPHA:411602Hereditary late-onset Parkinson disease8
HP:0000738HP:0000738Hallucinations0GLUD2 CL E G H27474336OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional1
HP:0000738HP:0000738Hallucinations0GRN CL E G H28964601OMIM:607485Frontotemporal lobar degeneration with TDP43 inclusions.126
HP:0000738HP:0000738Hallucinations0HARS1 CL E G H30354816ORPHA:231183Usher syndrome type 3HP:0040283 - Occasional
HP:0000738HP:0000738Hallucinations0HCRT CL E G H30604847OMIM:161400Narcolepsy 11
HP:0000738HP:0000738Hallucinations0HCRT CL E G H30604847ORPHA:2073Narcolepsy type 1HP:0040281 - Very frequent1
HP:0000738HP:0000738Hallucinations0HCRT CL E G H30604847ORPHA:83465Narcolepsy type 2HP:0040281 - Very frequent1
HP:0000738HP:0000738Hallucinations0HLA-DQB1 CL E G H31194944OMIM:123400Creutzfeldt-Jakob disease.
HP:0000738HP:0000738Hallucinations0HLA-DQB1 CL E G H31194944ORPHA:2073Narcolepsy type 1HP:0040281 - Very frequent
HP:0000738HP:0000738Hallucinations0HLA-DQB1 CL E G H31194944ORPHA:83465Narcolepsy type 2HP:0040281 - Very frequent
HP:0000738HP:0000738Hallucinations0HLA-DRB1 CL E G H31234948ORPHA:2073Narcolepsy type 1HP:0040281 - Very frequent2
HP:0000738HP:0000738Hallucinations0HLA-DRB1 CL E G H31234948ORPHA:83465Narcolepsy type 2HP:0040281 - Very frequent2
HP:0000738HP:0000738Hallucinations0HMBS CL E G H31454982ORPHA:79276Acute intermittent porphyriaHP:0040283 - Occasional81
HP:0000738HP:0000738Hallucinations0HTR2A CL E G H33565293OMIM:181500SCHIZOPHRENIA.4
HP:0000738HP:0000738Hallucinations0HTRA1 CL E G H56549476OMIM:600142Autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)34
HP:0000738HP:0000738Hallucinations0HTRA2 CL E G H2742914348ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent39
HP:0000738HP:0000738Hallucinations0HTT CL E G H30644851ORPHA:399Huntington diseaseHP:0040282 - Frequent12
HP:0000738HP:0000738Hallucinations0JPH3 CL E G H5733814203OMIM:606438Huntington disease-like 2.2
HP:0000738HP:0000738Hallucinations0KRAS CL E G H38456407ORPHA:144Lynch syndromeHP:0040283 - Occasional196
HP:0000738HP:0000738Hallucinations0LGI1 CL E G H92116572ORPHA:101046Autosomal dominant epilepsy with auditory features75
HP:0000738HP:0000738Hallucinations0LRRK2 CL E G H12089218618ORPHA:411602Hereditary late-onset Parkinson disease221
HP:0000738HP:0000738Hallucinations0LRRK2 CL E G H12089218618ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent221
HP:0000738HP:0000738Hallucinations0MAN2B1 CL E G H41256826ORPHA:309288Alpha-mannosidosis, adult formHP:0040283 - Occasional136
HP:0000738HP:0000738Hallucinations0MAN2B1 CL E G H41256826ORPHA:309282Alpha-mannosidosis, infantile formHP:0040283 - Occasional136
HP:0000738HP:0000738Hallucinations0MAPT CL E G H41376893OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional140
HP:0000738HP:0000738Hallucinations0MED12 CL E G H996811957ORPHA:776Lujan-Fryns syndromeHP:0040283 - Occasional228
HP:0000738HP:0000738Hallucinations0MLH1 CL E G H42927127ORPHA:144Lynch syndromeHP:0040283 - Occasional1819
HP:0000738HP:0000738Hallucinations0MLH3 CL E G H270307128ORPHA:144Lynch syndromeHP:0040283 - Occasional131
HP:0000738HP:0000738Hallucinations0MMACHC CL E G H2597424525ORPHA:79282Methylmalonic acidemia with homocystinuria, type cblC101
HP:0000738HP:0000738Hallucinations0MOG CL E G H43407197ORPHA:2073Narcolepsy type 1HP:0040281 - Very frequent1
HP:0000738HP:0000738Hallucinations0MSH2 CL E G H44367325ORPHA:144Lynch syndromeHP:0040283 - Occasional2162
HP:0000738HP:0000738Hallucinations0MSH6 CL E G H29567329ORPHA:144Lynch syndromeHP:0040283 - Occasional2232
HP:0000738HP:0000738Hallucinations0MTHFR CL E G H45247436OMIM:181500SCHIZOPHRENIA.183
HP:0000738HP:0000738Hallucinations0MYO7A CL E G H46477606ORPHA:231169Usher syndrome type 1HP:0040283 - Occasional516
HP:0000738HP:0000738Hallucinations0MYO7A CL E G H46477606ORPHA:231178Usher syndrome type 2HP:0040283 - Occasional516
HP:0000738HP:0000738Hallucinations0NDP CL E G H46937678ORPHA:649Norrie diseaseHP:0040283 - Occasional39
HP:0000738HP:0000738Hallucinations0NDP CL E G H46937678OMIM:310600Norrie disease.39
HP:0000738HP:0000738Hallucinations0NHLRC1 CL E G H37888421576ORPHA:501Lafora disease77
HP:0000738HP:0000738Hallucinations0NHLRC1 CL E G H37888421576OMIM:254780Myoclonic epilepsy of lafora77
HP:0000738HP:0000738Hallucinations0NPRL2 CL E G H1064124969ORPHA:98820Familial focal epilepsy with variable foci4
HP:0000738HP:0000738Hallucinations0NPRL3 CL E G H813114124ORPHA:98820Familial focal epilepsy with variable foci7
HP:0000738HP:0000738Hallucinations0NR4A2 CL E G H49297981OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional27
HP:0000738HP:0000738Hallucinations0OPA1 CL E G H49768140ORPHA:98673Autosomal dominant optic atrophy, classic formHP:0040284 - Very rare214
HP:0000738HP:0000738Hallucinations0P2RY11 CL E G H50328540ORPHA:2073Narcolepsy type 1HP:0040281 - Very frequent2
HP:0000738HP:0000738Hallucinations0PARK7 CL E G H1131516369ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent23
HP:0000738HP:0000738Hallucinations0PCDH15 CL E G H6521714674ORPHA:231169Usher syndrome type 1HP:0040283 - Occasional352
HP:0000738HP:0000738Hallucinations0PDZD7 CL E G H7995526257ORPHA:231178Usher syndrome type 2HP:0040283 - Occasional40
HP:0000738HP:0000738Hallucinations0PIK3CA CL E G H52908975ORPHA:144Lynch syndromeHP:0040283 - Occasional162
HP:0000738HP:0000738Hallucinations0PINK1 CL E G H6501814581ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent55
HP:0000738HP:0000738Hallucinations0PMS1 CL E G H53789121ORPHA:144Lynch syndromeHP:0040283 - Occasional56
HP:0000738HP:0000738Hallucinations0PMS2 CL E G H53959122ORPHA:144Lynch syndromeHP:0040283 - Occasional1121
HP:0000738HP:0000738Hallucinations0PODXL CL E G H54209171ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent6
HP:0000738HP:0000738Hallucinations0PPOX CL E G H54989280ORPHA:79473Porphyria variegataHP:0040284 - Very rare41
HP:0000738HP:0000738Hallucinations0PPT1 CL E G H55389325OMIM:256730Ceroid lipofuscinosis, neuronal, 1.172
HP:0000738HP:0000738Hallucinations0PRDM8 CL E G H5697813993OMIM:616640Epilepsy, progressive myoclonic, 101
HP:0000738HP:0000738Hallucinations0PRKN CL E G H50718607ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent138
HP:0000738HP:0000738Hallucinations0PRNP CL E G H56219449OMIM:123400Creutzfeldt-Jakob disease.69
HP:0000738HP:0000738Hallucinations0PRNP CL E G H56219449ORPHA:282166Inherited Creutzfeldt-Jakob diseaseHP:0040283 - Occasional69
HP:0000738HP:0000738Hallucinations0PSAP CL E G H56609498ORPHA:309271Metachromatic leukodystrophy, adult formHP:0040282 - Frequent81
HP:0000738HP:0000738Hallucinations0PSAP CL E G H56609498ORPHA:309263Metachromatic leukodystrophy, juvenile formHP:0040283 - Occasional81
HP:0000738HP:0000738Hallucinations0PSAP CL E G H56609498ORPHA:309256Metachromatic leukodystrophy, late infantile formHP:0040283 - Occasional81
HP:0000738HP:0000738Hallucinations0PSEN1 CL E G H56639508ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040281 - Very frequent241
HP:0000738HP:0000738Hallucinations0PSEN2 CL E G H56649509ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040281 - Very frequent59
HP:0000738HP:0000738Hallucinations0PSMD12 CL E G H57189557ORPHA:52996217q24.2 microdeletion syndromeHP:0040283 - Occasional4
HP:0000738HP:0000738Hallucinations0PUS3 CL E G H8348025461ORPHA:488627Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome1
HP:0000738HP:0000738Hallucinations0RELN CL E G H56499957ORPHA:101046Autosomal dominant epilepsy with auditory features334
HP:0000738HP:0000738Hallucinations0RPS20 CL E G H622410405ORPHA:440437Familial colorectal cancer Type XHP:0040283 - Occasional1
HP:0000738HP:0000738Hallucinations0RTN4R CL E G H6507818601OMIM:181500SCHIZOPHRENIA.2
HP:0000738HP:0000738Hallucinations0SEMA4A CL E G H6421810729ORPHA:440437Familial colorectal cancer Type XHP:0040283 - Occasional48
HP:0000738HP:0000738Hallucinations0SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type IIHP:0040282 - Frequent82
HP:0000738HP:0000738Hallucinations0SLC2A3 CL E G H651511007ORPHA:399Huntington diseaseHP:0040282 - Frequent1
HP:0000738HP:0000738Hallucinations0SLC6A19 CL E G H34002427960ORPHA:2116Hartnup diseaseHP:0040281 - Very frequent12
HP:0000738HP:0000738Hallucinations0SNCA CL E G H662211138OMIM:127750Dementia, lewy body65
HP:0000738HP:0000738Hallucinations0SNCA CL E G H662211138ORPHA:411602Hereditary late-onset Parkinson disease65
HP:0000738HP:0000738Hallucinations0SNCA CL E G H662211138OMIM:168601Parkinson disease 1, autosomal dominant.65
HP:0000738HP:0000738Hallucinations0SNCA CL E G H662211138OMIM:605543Parkinson disease 4.65
HP:0000738HP:0000738Hallucinations0SNCA CL E G H662211138ORPHA:171695Parkinsonian-pyramidal syndrome65
HP:0000738HP:0000738Hallucinations0SNCA CL E G H662211138ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent65
HP:0000738HP:0000738Hallucinations0SNCAIP CL E G H962711139OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional35
HP:0000738HP:0000738Hallucinations0SNCB CL E G H662011140OMIM:127750Dementia, lewy body2
HP:0000738HP:0000738Hallucinations0SON CL E G H665111183ORPHA:500150Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome12
HP:0000738HP:0000738Hallucinations0SORL1 CL E G H665311185ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040281 - Very frequent3
HP:0000738HP:0000738Hallucinations0SPART CL E G H2311118514ORPHA:101000Autosomal recessive spastic paraplegia type 20HP:0040283 - Occasional66
HP:0000738HP:0000738Hallucinations0SQSTM1 CL E G H887811280ORPHA:275872Frontotemporal dementia with motor neuron diseaseHP:0040282 - Frequent62
HP:0000738HP:0000738Hallucinations0SYN2 CL E G H685411495OMIM:181500SCHIZOPHRENIA.3
HP:0000738HP:0000738Hallucinations0SYNJ1 CL E G H886711503ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent9
HP:0000738HP:0000738Hallucinations0TARDBP CL E G H2343511571ORPHA:275872Frontotemporal dementia with motor neuron diseaseHP:0040282 - Frequent65
HP:0000738HP:0000738Hallucinations0TBK1 CL E G H2911011584ORPHA:275872Frontotemporal dementia with motor neuron diseaseHP:0040282 - Frequent20
HP:0000738HP:0000738Hallucinations0TBP CL E G H690811588OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional7
HP:0000738HP:0000738Hallucinations0TBP CL E G H690811588OMIM:607136Spinocerebellar ataxia 17.7
HP:0000738HP:0000738Hallucinations0TGFBR2 CL E G H704811773ORPHA:144Lynch syndromeHP:0040283 - Occasional253
HP:0000738HP:0000738Hallucinations0TNFSF4 CL E G H729211934ORPHA:2073Narcolepsy type 1HP:0040281 - Very frequent
HP:0000738HP:0000738Hallucinations0TOMM40 CL E G H1045218001ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040281 - Very frequent
HP:0000738HP:0000738Hallucinations0TREM2 CL E G H5420917761ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040281 - Very frequent31
HP:0000738HP:0000738Hallucinations0TRNS2 CL E G H45757498ORPHA:231183Usher syndrome type 3HP:0040283 - Occasional
HP:0000738HP:0000738Hallucinations0TRNT CL E G H45767499OMIM:168600Parkinson disease, late-onsetHP:0040283 - Occasional
HP:0000738HP:0000738Hallucinations0TRRAP CL E G H829512347OMIM:618454Developmental delay with or without dysmorphic facies and autism2
HP:0000738HP:0000738Hallucinations0TTC19 CL E G H5490226006OMIM:615157Mitochondrial complex III deficiency, nuclear type 2.88
HP:0000738HP:0000738Hallucinations0UCHL1 CL E G H734512513ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent21
HP:0000738HP:0000738Hallucinations0UPF3B CL E G H6510920439ORPHA:776Lujan-Fryns syndromeHP:0040283 - Occasional33
HP:0000738HP:0000738Hallucinations0USH1C CL E G H1008312597ORPHA:231169Usher syndrome type 1HP:0040283 - Occasional173
HP:0000738HP:0000738Hallucinations0USH1G CL E G H12459016356ORPHA:231169Usher syndrome type 1HP:0040283 - Occasional78
HP:0000738HP:0000738Hallucinations0USH2A CL E G H739912601ORPHA:231178Usher syndrome type 2HP:0040283 - Occasional777
HP:0000738HP:0000738Hallucinations0VCP CL E G H741512666ORPHA:275872Frontotemporal dementia with motor neuron diseaseHP:0040282 - Frequent63
HP:0000738HP:0000738Hallucinations0VPS13C CL E G H5483223594ORPHA:2828Young-onset Parkinson diseaseHP:0040282 - Frequent8
HP:0000738HP:0000738Hallucinations0VPS35 CL E G H5573713487ORPHA:411602Hereditary late-onset Parkinson disease37
HP:0000738HP:0000738Hallucinations0WFS1 CL E G H746612762ORPHA:3463Wolfram syndromeHP:0040283 - Occasional389
HP:0000738HP:0000738Hallucinations0WHRN CL E G H2586116361ORPHA:231178Usher syndrome type 2HP:0040283 - Occasional155
HP:0000738HP:0000738Hallucinations0ZDHHC9 CL E G H5111418475ORPHA:776Lujan-Fryns syndromeHP:0040283 - Occasional10
HP:0000738HP:0000738Hallucinations0ZNF365 CL E G H2289118194ORPHA:2073Narcolepsy type 1HP:0040281 - Very frequent3
HP:0000738HP:0000738Hallucinations0ZNF365 CL E G H2289118194ORPHA:83465Narcolepsy type 2HP:0040281 - Very frequent3
HP:0000738HP:0033694Tactile hallucination1 CL E G H
HP:0000738HP:0006803Vivid hallucinations1 CL E G H
HP:0000738HP:0002367Visual hallucinations1ATP13A2 CL E G H2340030213ORPHA:306674Kufor-Rakeb syndromeHP:0040282 - Frequent100
HP:0000738HP:0002367Visual hallucinations1CACNA1A CL E G H7731388OMIM:141500Migraine, familial hemiplegic, 1.449
HP:0000738HP:0008765Auditory hallucinations1CACNA1A CL E G H7731388OMIM:141500Migraine, familial hemiplegic, 1.449
HP:0000738HP:0008765Auditory hallucinations1CDH2 CL E G H10001759OMIM:618929AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS
HP:0000738HP:0008765Auditory hallucinations1CEP85L CL E G H38711921638OMIM:618873LISSENCEPHALY 10; LIS101
HP:0000738HP:0002367Visual hallucinations1CLN3 CL E G H12012074ORPHA:228346CLN3 disease216
HP:0000738HP:0002367Visual hallucinations1CLN6 CL E G H549822077OMIM:204300Ceroid lipofuscinosis, neuronal, 4A, autosomal recessive.143
HP:0000738HP:0008765Auditory hallucinations1CLN6 CL E G H549822077OMIM:204300Ceroid lipofuscinosis, neuronal, 4A, autosomal recessive.143
HP:0000738HP:0008765Auditory hallucinations1CSF1R CL E G H14362433OMIM:221820Leukoencephalopathy, diffuse hereditary, with spheroids149
HP:0000738HP:0002367Visual hallucinations1DEPDC5 CL E G H968118423ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040283 - Occasional172
HP:0000738HP:0008765Auditory hallucinations1DEPDC5 CL E G H968118423ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040281 - Very frequent172
HP:0000738HP:0002367Visual hallucinations1DEPDC5 CL E G H968118423ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional172
HP:0000738HP:0008765Auditory hallucinations1DEPDC5 CL E G H968118423ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional172
HP:0000738HP:0002367Visual hallucinations1DNAJC13 CL E G H2331730343ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional2
HP:0000738HP:0002367Visual hallucinations1DNAJC5 CL E G H8033116235OMIM:162350Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant.155
HP:0000738HP:0008765Auditory hallucinations1DNAJC5 CL E G H8033116235OMIM:162350Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant.155
HP:0000738HP:0002367Visual hallucinations1EIF4G1 CL E G H19813296ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional2
HP:0000738HP:0002367Visual hallucinations1EPM2A CL E G H79573413ORPHA:501Lafora diseaseHP:0040282 - Frequent83
HP:0000738HP:0002367Visual hallucinations1EPM2A CL E G H79573413OMIM:254780Myoclonic epilepsy of lafora.83
HP:0000738HP:0002367Visual hallucinations1FBXO7 CL E G H2579313586ORPHA:171695Parkinsonian-pyramidal syndromeHP:0040282 - Frequent36
HP:0000738HP:0002367Visual hallucinations1FIG4 CL E G H989616873ORPHA:208441Bilateral parasagittal parieto-occipital polymicrogyriaHP:0040283 - Occasional111
HP:0000738HP:0008765Auditory hallucinations1FIG4 CL E G H989616873ORPHA:208441Bilateral parasagittal parieto-occipital polymicrogyriaHP:0040283 - Occasional111
HP:0000738HP:0002367Visual hallucinations1FIG4 CL E G H989616873OMIM:612691Polymicrogyria, bilateral temporooccipital.111
HP:0000738HP:0002367Visual hallucinations1GBA1 CL E G H26294177OMIM:127750Dementia, lewy body.
HP:0000738HP:0002367Visual hallucinations1GBA1 CL E G H26294177ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional
HP:0000738HP:0002367Visual hallucinations1GIGYF2 CL E G H2605811960ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional8
HP:0000738HP:0006896Hypnopompic hallucinations1HCRT CL E G H30604847OMIM:161400Narcolepsy 1.1
HP:0000738HP:0002519Hypnagogic hallucinations1HCRT CL E G H30604847OMIM:161400Narcolepsy 1.1
HP:0000738HP:0002367Visual hallucinations1LGI1 CL E G H92116572ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040283 - Occasional75
HP:0000738HP:0008765Auditory hallucinations1LGI1 CL E G H92116572ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040281 - Very frequent75
HP:0000738HP:0002367Visual hallucinations1LRRK2 CL E G H12089218618ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional221
HP:0000738HP:0008765Auditory hallucinations1MMACHC CL E G H2597424525ORPHA:79282Methylmalonic acidemia with homocystinuria, type cblCHP:0040283 - Occasional101
HP:0000738HP:0002367Visual hallucinations1NHLRC1 CL E G H37888421576ORPHA:501Lafora diseaseHP:0040282 - Frequent77
HP:0000738HP:0002367Visual hallucinations1NHLRC1 CL E G H37888421576OMIM:254780Myoclonic epilepsy of lafora.77
HP:0000738HP:0002367Visual hallucinations1NPRL2 CL E G H1064124969ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional4
HP:0000738HP:0008765Auditory hallucinations1NPRL2 CL E G H1064124969ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional4
HP:0000738HP:0008765Auditory hallucinations1NPRL3 CL E G H813114124ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional7
HP:0000738HP:0002367Visual hallucinations1NPRL3 CL E G H813114124ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional7
HP:0000738HP:0002367Visual hallucinations1PUS3 CL E G H8348025461ORPHA:488627Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndromeHP:0040283 - Occasional1
HP:0000738HP:0002367Visual hallucinations1RELN CL E G H56499957ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040283 - Occasional334
HP:0000738HP:0008765Auditory hallucinations1RELN CL E G H56499957ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040281 - Very frequent334
HP:0000738HP:0002367Visual hallucinations1SNCA CL E G H662211138OMIM:127750Dementia, lewy body.65
HP:0000738HP:0002367Visual hallucinations1SNCA CL E G H662211138ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional65
HP:0000738HP:0002367Visual hallucinations1SNCA CL E G H662211138ORPHA:171695Parkinsonian-pyramidal syndromeHP:0040282 - Frequent65
HP:0000738HP:0002367Visual hallucinations1SNCB CL E G H662011140OMIM:127750Dementia, lewy body.2
HP:0000738HP:0008765Auditory hallucinations1SON CL E G H665111183ORPHA:500150Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndromeHP:0040283 - Occasional12
HP:0000738HP:0002367Visual hallucinations1VPS35 CL E G H5573713487ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional37


Genes (150) :ABCA7 ADGRV1 ADH1C ALAD ALDH4A1 ALDH5A1 APOL2 APOL4 APP ARSA ARSG ATP13A2 ATXN2 ATXN8OS BCKDHA BCKDHB BCS1L BMPR1A BPTF C9ORF72 CACNA1A CDH2 CDH23 CEP78 CEP85L CHCHD10 CHI3L1 CIB2 CISD2 CLN3 CLN5 CLN6 CLRN1 CLTRN COMT CPOX CSF1R CTSH CYP27A1 DAOA DBT DCAF17 DEPDC5 DISC2 DNAJC13 DNAJC5 DNAJC6 DNM1L DRD3 ECM1 EIF4G1 EPCAM EPM2A ESPN FAN1 FBXO7 FIG4 FUS GBA1 GIGYF2 GLUD2 GRN HARS1 HCRT HLA-DQB1 HLA-DRB1 HMBS HTR2A HTRA1 HTRA2 HTT JPH3 KRAS LGI1 LRRK2 MAN2B1 MAPT MED12 MLH1 MLH3 MMACHC MOG MSH2 MSH6 MTHFR MYO7A NDP NHLRC1 NPRL2 NPRL3 NR4A2 OPA1 P2RY11 PARK7 PCDH15 PDZD7 PIK3CA PINK1 PMS1 PMS2 PODXL PPOX PPT1 PRDM8 PRKN PRNP PSAP PSEN1 PSEN2 PSMD12 PUS3 RELN RPS20 RTN4R SEMA4A SLC25A13 SLC2A3 SLC6A19 SNCA SNCAIP SNCB SON SORL1 SPART SQSTM1 SYN2 SYNJ1 TARDBP TBK1 TBP TGFBR2 TNFSF4 TOMM40 TREM2 TRNS2 TRNT TRRAP TTC19 UCHL1 UPF3B USH1C USH1G USH2A VCP VPS13C VPS35 WFS1 WHRN ZDHHC9 ZNF365

Diseases (80) :ORPHA:1020 ORPHA:231178 OMIM:168600 ORPHA:100924 ORPHA:79101 OMIM:271980 OMIM:181500 OMIM:250100 ORPHA:309271 ORPHA:309263 ORPHA:309256 ORPHA:231183 ORPHA:513436 ORPHA:306674 OMIM:606693 OMIM:617225 OMIM:248600 OMIM:124000 ORPHA:440437 ORPHA:529962 OMIM:105550 ORPHA:275872 OMIM:141500 OMIM:618929 ORPHA:231169 OMIM:618873 ORPHA:3463 ORPHA:228346 ORPHA:228360 OMIM:204300 ORPHA:2116 OMIM:121300 OMIM:221820 ORPHA:2073 ORPHA:909 OMIM:213700 ORPHA:3464 OMIM:241080 ORPHA:101046 ORPHA:98820 ORPHA:411602 OMIM:162350 OMIM:615528 ORPHA:2828 ORPHA:98673 OMIM:247100 ORPHA:144 ORPHA:501 OMIM:254780 ORPHA:171695 ORPHA:208441 OMIM:612691 OMIM:127750 OMIM:607485 OMIM:161400 ORPHA:83465 OMIM:123400 ORPHA:79276 OMIM:600142 ORPHA:399 OMIM:606438 ORPHA:309288 ORPHA:309282 ORPHA:776 ORPHA:79282 ORPHA:649 OMIM:310600 ORPHA:79473 OMIM:256730 OMIM:616640 ORPHA:282166 ORPHA:488627 ORPHA:247585 OMIM:168601 OMIM:605543 ORPHA:500150 ORPHA:101000 OMIM:607136 OMIM:618454 OMIM:615157
 

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