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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Auditory hallucinations (HP:0008765)help
Term ID: 8765
Name: Auditory hallucinations
Synonym: Hallucinations of sound; Hearing sounds
Definition: The false perception of sound.
Comments:
Reference: HP:0008765
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHypnagogic hallucinations (HP:0002519) help
..expandHypnopompic hallucinations (HP:0006896) help
..expandVisual hallucinations (HP:0002367) 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:0008765HP:0008765Auditory hallucinations0CACNA1A CL E G H7731388OMIM:141500Migraine, familial hemiplegic, 1.449
HP:0008765HP:0008765Auditory hallucinations0CDH2 CL E G H10001759OMIM:618929AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS
HP:0008765HP:0008765Auditory hallucinations0CEP85L CL E G H38711921638OMIM:618873LISSENCEPHALY 10; LIS101
HP:0008765HP:0008765Auditory hallucinations0CLN6 CL E G H549822077OMIM:204300Ceroid lipofuscinosis, neuronal, 4A, autosomal recessive.143
HP:0008765HP:0008765Auditory hallucinations0CSF1R CL E G H14362433OMIM:221820Leukoencephalopathy, diffuse hereditary, with spheroids149
HP:0008765HP:0008765Auditory hallucinations0DEPDC5 CL E G H968118423ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040281 - Very frequent172
HP:0008765HP:0008765Auditory hallucinations0DEPDC5 CL E G H968118423ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional172
HP:0008765HP:0008765Auditory hallucinations0DNAJC5 CL E G H8033116235OMIM:162350Ceroid lipofuscinosis, neuronal, 4B, autosomal dominant.155
HP:0008765HP:0008765Auditory hallucinations0FIG4 CL E G H989616873ORPHA:208441Bilateral parasagittal parieto-occipital polymicrogyriaHP:0040283 - Occasional111
HP:0008765HP:0008765Auditory hallucinations0LGI1 CL E G H92116572ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040281 - Very frequent75
HP:0008765HP:0008765Auditory hallucinations0MMACHC CL E G H2597424525ORPHA:79282Methylmalonic acidemia with homocystinuria, type cblCHP:0040283 - Occasional101
HP:0008765HP:0008765Auditory hallucinations0NPRL2 CL E G H1064124969ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional4
HP:0008765HP:0008765Auditory hallucinations0NPRL3 CL E G H813114124ORPHA:98820Familial focal epilepsy with variable fociHP:0040283 - Occasional7
HP:0008765HP:0008765Auditory hallucinations0RELN CL E G H56499957ORPHA:101046Autosomal dominant epilepsy with auditory featuresHP:0040281 - Very frequent334
HP:0008765HP:0008765Auditory hallucinations0SON CL E G H665111183ORPHA:500150Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndromeHP:0040283 - Occasional12


Genes (14) :CACNA1A CDH2 CEP85L CLN6 CSF1R DEPDC5 DNAJC5 FIG4 LGI1 MMACHC NPRL2 NPRL3 RELN SON

Diseases (11) :OMIM:141500 OMIM:618929 OMIM:618873 OMIM:204300 OMIM:221820 ORPHA:101046 ORPHA:98820 OMIM:162350 ORPHA:208441 ORPHA:79282 ORPHA:500150
 

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