Human Phenotype Ontology 
Grandparent Node:
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Behavioral abnormality (HP:0000708)help
Parent Node:
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Hallucinations (HP:0000738)help
..Starting node
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Visual hallucinations (HP:0002367)help
Term ID: 2367
Name: Visual hallucinations
Synonym: Visual hallucinations
Definition: Visual perceptions that are not elicited by a corresponding stimulus from the outside world.
Comments:
Reference: HP:0002367
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAuditory hallucinations (HP:0008765) help
..expandHypnagogic hallucinations (HP:0002519) help
..expandHypnopompic hallucinations (HP:0006896) help
..expandVivid hallucinations (HP:0006803) 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:0002367HP:0002367Visual hallucinations0ATP13A2 CL E G H2340030213ORPHA:306674Kufor-Rakeb syndromeHP:0040282 - Frequent100
HP:0002367HP:0002367Visual hallucinations0CACNA1A CL E G H7731388OMIM:141500Migraine, familial hemiplegic, 1.449
HP:0002367HP:0002367Visual hallucinations0CLN3 CL E G H12012074ORPHA:228346CLN3 disease216
HP:0002367HP:0002367Visual hallucinations0CLN6 CL E G H549822077OMIM:204300Ceroid lipofuscinosis, neuronal, 4A, autosomal recessive.143
HP:0002367HP:0002367Visual hallucinations0DEPDC5 CL E G H968118423ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040283 - Occasional172
HP:0002367HP:0002367Visual hallucinations0DEPDC5 CL E G H968118423ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional172
HP:0002367HP:0002367Visual hallucinations0DNAJC13 CL E G H2331730343ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional2
HP:0002367HP:0002367Visual hallucinations0DNAJC5 CL E G H8033116235OMIM:162350Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant.155
HP:0002367HP:0002367Visual hallucinations0EIF4G1 CL E G H19813296ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional2
HP:0002367HP:0002367Visual hallucinations0EPM2A CL E G H79573413ORPHA:501Lafora diseaseHP:0040282 - Frequent83
HP:0002367HP:0002367Visual hallucinations0EPM2A CL E G H79573413OMIM:254780Myoclonic epilepsy of lafora.83
HP:0002367HP:0002367Visual hallucinations0FBXO7 CL E G H2579313586ORPHA:171695Parkinsonian-pyramidal syndromeHP:0040282 - Frequent36
HP:0002367HP:0002367Visual hallucinations0FIG4 CL E G H989616873ORPHA:208441Bilateral parasagittal parieto-occipital polymicrogyriaHP:0040283 - Occasional111
HP:0002367HP:0002367Visual hallucinations0FIG4 CL E G H989616873OMIM:612691Polymicrogyria, bilateral temporooccipital.111
HP:0002367HP:0002367Visual hallucinations0GBA1 CL E G H26294177OMIM:127750Dementia, lewy body.
HP:0002367HP:0002367Visual hallucinations0GBA1 CL E G H26294177ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional
HP:0002367HP:0002367Visual hallucinations0GIGYF2 CL E G H2605811960ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional8
HP:0002367HP:0002367Visual hallucinations0LGI1 CL E G H92116572ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040283 - Occasional75
HP:0002367HP:0002367Visual hallucinations0LRRK2 CL E G H12089218618ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional221
HP:0002367HP:0002367Visual hallucinations0NHLRC1 CL E G H37888421576ORPHA:501Lafora diseaseHP:0040282 - Frequent77
HP:0002367HP:0002367Visual hallucinations0NHLRC1 CL E G H37888421576OMIM:254780Myoclonic epilepsy of lafora.77
HP:0002367HP:0002367Visual hallucinations0NPRL2 CL E G H1064124969ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional4
HP:0002367HP:0002367Visual hallucinations0NPRL3 CL E G H813114124ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional7
HP:0002367HP:0002367Visual hallucinations0PUS3 CL E G H8348025461ORPHA:488627Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndromeHP:0040283 - Occasional1
HP:0002367HP:0002367Visual hallucinations0RELN CL E G H56499957ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040283 - Occasional334
HP:0002367HP:0002367Visual hallucinations0SNCA CL E G H662211138OMIM:127750Dementia, lewy body.65
HP:0002367HP:0002367Visual hallucinations0SNCA CL E G H662211138ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional65
HP:0002367HP:0002367Visual hallucinations0SNCA CL E G H662211138ORPHA:171695Parkinsonian-pyramidal syndromeHP:0040282 - Frequent65
HP:0002367HP:0002367Visual hallucinations0SNCB CL E G H662011140OMIM:127750Dementia, lewy body.2
HP:0002367HP:0002367Visual hallucinations0VPS35 CL E G H5573713487ORPHA:411602Hereditary late-onset Parkinson diseaseHP:0040283 - Occasional37


Genes (23) :ATP13A2 CACNA1A CLN3 CLN6 DEPDC5 DNAJC13 DNAJC5 EIF4G1 EPM2A FBXO7 FIG4 GBA1 GIGYF2 LGI1 LRRK2 NHLRC1 NPRL2 NPRL3 PUS3 RELN SNCA SNCB VPS35

Diseases (15) :ORPHA:306674 OMIM:141500 ORPHA:228346 OMIM:204300 ORPHA:101046 ORPHA:98820 ORPHA:411602 OMIM:162350 ORPHA:501 OMIM:254780 ORPHA:171695 ORPHA:208441 OMIM:612691 OMIM:127750 ORPHA:488627
 

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