Human Phenotype Ontology 
Grandparent Node:
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Abnormal ear physiology (HP:0031704)help
Parent Node:
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Hearing abnormality (HP:0000364)help
..Starting node
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Tinnitus (HP:0000360)help
Term ID: 360
Name: Tinnitus
Synonym: Ringing in ears; Ringing in the ears
Definition: Tinnitus is an auditory perception that can be described as the experience of sound, in the ear or in the head, in the absence of external acoustic stimulation.
Comments:
Reference: HP:0000360
Genes and Diseases:
 
       Child Nodes:
........expandPulsatile tinnitus (HP:0008629) help

 Sister Nodes: 
..expandAbnormal speech discrimination (HP:0001963) help
..expandHearing impairment (HP:0000365) 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:0000360HP:0000360Tinnitus0AIFM1 CL E G H91318768OMIM:300614Deafness, X-linked 5.60
HP:0000360HP:0000360Tinnitus0AKT1 CL E G H207391ORPHA:2495MeningiomaHP:0040284 - Very rare54
HP:0000360HP:0000360Tinnitus0ATP1A2 CL E G H477800ORPHA:569Familial or sporadic hemiplegic migraineHP:0040283 - Occasional239
HP:0000360HP:0000360Tinnitus0ATP2B2 CL E G H491815OMIM:619804DEAFNESS, AUTOSOMAL DOMINANT 82; DFNA825
HP:0000360HP:0000360Tinnitus0BAP1 CL E G H8314950ORPHA:2495MeningiomaHP:0040284 - Very rare184
HP:0000360HP:0000360Tinnitus0CACNA1A CL E G H7731388OMIM:108500Episodic ataxia, type 2.449
HP:0000360HP:0000360Tinnitus0CACNA1A CL E G H7731388ORPHA:569Familial or sporadic hemiplegic migraineHP:0040283 - Occasional449
HP:0000360HP:0000360Tinnitus0CACNA1A CL E G H7731388ORPHA:97Familial paroxysmal ataxiaHP:0040282 - Frequent449
HP:0000360HP:0000360Tinnitus0CACNA1D CL E G H7761391ORPHA:369929Primary hyperaldosteronism-seizures-neurological abnormalities syndromeHP:0040283 - Occasional51
HP:0000360HP:0000360Tinnitus0CAV1 CL E G H8571527OMIM:606721Lipodystrophy, familial partial, type 711
HP:0000360HP:0000360Tinnitus0CCND1 CL E G H5951582OMIM:193300Von hippel-lindau syndrome.1
HP:0000360HP:0000360Tinnitus0CLCN2 CL E G H11812020ORPHA:404Familial hyperaldosteronism type IIHP:0040283 - Occasional44
HP:0000360HP:0000360Tinnitus0CLCNKB CL E G H11882027ORPHA:358Gitelman syndromeHP:0040284 - Very rare27
HP:0000360HP:0000360Tinnitus0COCH CL E G H16902180OMIM:601369Deafness, autosomal dominant 9.46
HP:0000360HP:0000360Tinnitus0CYP11B1 CL E G H15842591ORPHA:403Familial hyperaldosteronism type IHP:0040283 - Occasional112
HP:0000360HP:0000360Tinnitus0CYP11B2 CL E G H15852592ORPHA:403Familial hyperaldosteronism type IHP:0040283 - Occasional73
HP:0000360HP:0000360Tinnitus0DIABLO CL E G H5661621528OMIM:614152Deafness, autosomal dominant 64.11
HP:0000360HP:0000360Tinnitus0DKK1 CL E G H229432891ORPHA:268882Arnold-Chiari malformation type IHP:0040282 - Frequent
HP:0000360HP:0000360Tinnitus0DLST CL E G H17432911ORPHA:29072Hereditary pheochromocytoma-paraganglioma
HP:0000360HP:0000360Tinnitus0DNMT3A CL E G H17882978ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma44
HP:0000360HP:0000360Tinnitus0DSPP CL E G H18343054OMIM:605594Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1.38
HP:0000360HP:0000360Tinnitus0EPAS1 CL E G H20343374ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma112
HP:0000360HP:0000360Tinnitus0FH CL E G H22713700ORPHA:29072Hereditary pheochromocytoma-paraganglioma301
HP:0000360HP:0000360Tinnitus0GRM1 CL E G H29114593OMIM:617691SPINOCEREBELLAR ATAXIA 44; SCA448
HP:0000360HP:0000360Tinnitus0JAK2 CL E G H37176192ORPHA:729Polycythemia veraHP:0040281 - Very frequent57
HP:0000360HP:0000360Tinnitus0KCNJ5 CL E G H37626266ORPHA:251274Familial hyperaldosteronism type IIIHP:0040283 - Occasional128
HP:0000360HP:0000360Tinnitus0KCNQ4 CL E G H91326298OMIM:600101Deafness, autosomal dominant nonsyndromic sensorineural 2.76
HP:0000360HP:0000360Tinnitus0KIF1B CL E G H2309516636ORPHA:29072Hereditary pheochromocytoma-paraganglioma202
HP:0000360HP:0000360Tinnitus0MAX CL E G H41496913ORPHA:29072Hereditary pheochromocytoma-paraganglioma84
HP:0000360HP:0000360Tinnitus0MDH2 CL E G H41916971ORPHA:29072Hereditary pheochromocytoma-paraganglioma4
HP:0000360HP:0000360Tinnitus0MFN2 CL E G H992716877OMIM:601152Hereditary motor and sensory neuropathy VI.203
HP:0000360HP:0000360Tinnitus0MIR96 CL E G H40705331648OMIM:613074Deafness, autosomal dominant 50HP:0040283 - Occasional4
HP:0000360HP:0000360Tinnitus0MPL CL E G H43527217ORPHA:729Polycythemia veraHP:0040281 - Very frequent97
HP:0000360HP:0000360Tinnitus0NAGA CL E G H46687631ORPHA:79280Alpha-N-acetylgalactosaminidase deficiency type 2HP:0040282 - Frequent47
HP:0000360HP:0000360Tinnitus0NF1 CL E G H47637765ORPHA:29072Hereditary pheochromocytoma-paraganglioma1952
HP:0000360HP:0000360Tinnitus0NF2 CL E G H47717773ORPHA:2495MeningiomaHP:0040284 - Very rare220
HP:0000360HP:0000360Tinnitus0NF2 CL E G H47717773ORPHA:637Neurofibromatosis type 2HP:0040283 - Occasional220
HP:0000360HP:0000360Tinnitus0NF2 CL E G H47717773OMIM:101000Neurofibromatosis, type II220
HP:0000360HP:0000360Tinnitus0OSBPL2 CL E G H988515761OMIM:616340DEAFNESS, AUTOSOMAL DOMINANT 67; DFNA672
HP:0000360HP:0000360Tinnitus0P2RX2 CL E G H2295315459OMIM:608224Deafness, autosomal dominant 41.23
HP:0000360HP:0000360Tinnitus0PDGFB CL E G H51558800ORPHA:2495MeningiomaHP:0040284 - Very rare9
HP:0000360HP:0000360Tinnitus0PIK3CA CL E G H52908975ORPHA:2495MeningiomaHP:0040284 - Very rare162
HP:0000360HP:0000360Tinnitus0PMP22 CL E G H53769118ORPHA:90658Charcot-Marie-Tooth disease type 1EHP:0040283 - Occasional79
HP:0000360HP:0000360Tinnitus0PRRT2 CL E G H11247630500ORPHA:569Familial or sporadic hemiplegic migraineHP:0040283 - Occasional94
HP:0000360HP:0000360Tinnitus0RET CL E G H59799967ORPHA:29072Hereditary pheochromocytoma-paraganglioma572
HP:0000360HP:0000360Tinnitus0RET CL E G H59799967ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma572
HP:0000360HP:0000360Tinnitus0SCN1A CL E G H632310585ORPHA:569Familial or sporadic hemiplegic migraineHP:0040283 - Occasional1053
HP:0000360HP:0000360Tinnitus0SDHA CL E G H638910680ORPHA:29072Hereditary pheochromocytoma-paraganglioma304
HP:0000360HP:0000360Tinnitus0SDHAF2 CL E G H5494926034ORPHA:29072Hereditary pheochromocytoma-paraganglioma55
HP:0000360HP:0000360Tinnitus0SDHAF2 CL E G H5494926034OMIM:601650Paragangliomas 255
HP:0000360HP:0000360Tinnitus0SDHB CL E G H639010681ORPHA:97286Carney-Stratakis syndromeHP:0040282 - Frequent237
HP:0000360HP:0000360Tinnitus0SDHB CL E G H639010681ORPHA:29072Hereditary pheochromocytoma-paraganglioma237
HP:0000360HP:0000360Tinnitus0SDHB CL E G H639010681OMIM:115310Paragangliomas 4237
HP:0000360HP:0000360Tinnitus0SDHB CL E G H639010681ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma237
HP:0000360HP:0000360Tinnitus0SDHC CL E G H639110682ORPHA:97286Carney-Stratakis syndromeHP:0040282 - Frequent147
HP:0000360HP:0000360Tinnitus0SDHC CL E G H639110682ORPHA:29072Hereditary pheochromocytoma-paraganglioma147
HP:0000360HP:0000360Tinnitus0SDHC CL E G H639110682OMIM:605373Paragangliomas 3147
HP:0000360HP:0000360Tinnitus0SDHD CL E G H639210683ORPHA:97286Carney-Stratakis syndromeHP:0040282 - Frequent129
HP:0000360HP:0000360Tinnitus0SDHD CL E G H639210683ORPHA:29072Hereditary pheochromocytoma-paraganglioma129
HP:0000360HP:0000360Tinnitus0SDHD CL E G H639210683OMIM:168000Paragangliomas 1129
HP:0000360HP:0000360Tinnitus0SDHD CL E G H639210683ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma129
HP:0000360HP:0000360Tinnitus0SLC12A3 CL E G H655910912ORPHA:358Gitelman syndromeHP:0040284 - Very rare145
HP:0000360HP:0000360Tinnitus0SLC25A11 CL E G H840210981ORPHA:29072Hereditary pheochromocytoma-paraganglioma
HP:0000360HP:0000360Tinnitus0SLC39A14 CL E G H2351620858OMIM:144755Hyperostosis cranialis interna.5
HP:0000360HP:0000360Tinnitus0SLC44A4 CL E G H8073613941OMIM:617606Deafness, autosomal dominant 72.1
HP:0000360HP:0000360Tinnitus0SMARCB1 CL E G H659811103ORPHA:2495MeningiomaHP:0040284 - Very rare87
HP:0000360HP:0000360Tinnitus0SMARCE1 CL E G H660511109ORPHA:2495MeningiomaHP:0040284 - Very rare47
HP:0000360HP:0000360Tinnitus0SMO CL E G H660811119ORPHA:2495MeningiomaHP:0040284 - Very rare22
HP:0000360HP:0000360Tinnitus0SUFU CL E G H5168416466ORPHA:2495MeningiomaHP:0040284 - Very rare124
HP:0000360HP:0000360Tinnitus0TERT CL E G H701511730ORPHA:2495MeningiomaHP:0040284 - Very rare238
HP:0000360HP:0000360Tinnitus0TET2 CL E G H5479025941ORPHA:729Polycythemia veraHP:0040281 - Very frequent3
HP:0000360HP:0000360Tinnitus0TMC1 CL E G H11753116513OMIM:606705Deafness, autosomal dominant 36.109
HP:0000360HP:0000360Tinnitus0TMEM127 CL E G H5565426038ORPHA:29072Hereditary pheochromocytoma-paraganglioma131
HP:0000360HP:0000360Tinnitus0TRAF7 CL E G H8423120456ORPHA:2495MeningiomaHP:0040284 - Very rare
HP:0000360HP:0000360Tinnitus0VHL CL E G H742812687ORPHA:29072Hereditary pheochromocytoma-paraganglioma490
HP:0000360HP:0000360Tinnitus0VHL CL E G H742812687ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma490
HP:0000360HP:0000360Tinnitus0VHL CL E G H742812687OMIM:193300Von hippel-lindau syndrome.490
HP:0000360HP:0034424Clicking tinnitus1 CL E G H
HP:0000360HP:0008629Pulsatile tinnitus1DLST CL E G H17432911ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent
HP:0000360HP:0008629Pulsatile tinnitus1DNMT3A CL E G H17882978ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent44
HP:0000360HP:0008629Pulsatile tinnitus1EPAS1 CL E G H20343374ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent112
HP:0000360HP:0008629Pulsatile tinnitus1FH CL E G H22713700ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent301
HP:0000360HP:0008629Pulsatile tinnitus1KIF1B CL E G H2309516636ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent202
HP:0000360HP:0008629Pulsatile tinnitus1MAX CL E G H41496913ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent84
HP:0000360HP:0008629Pulsatile tinnitus1MDH2 CL E G H41916971ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent4
HP:0000360HP:0008629Pulsatile tinnitus1NF1 CL E G H47637765ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent1952
HP:0000360HP:0008629Pulsatile tinnitus1RET CL E G H59799967ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent572
HP:0000360HP:0008629Pulsatile tinnitus1RET CL E G H59799967ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent572
HP:0000360HP:0008629Pulsatile tinnitus1SDHA CL E G H638910680ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent304
HP:0000360HP:0008629Pulsatile tinnitus1SDHAF2 CL E G H5494926034ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent55
HP:0000360HP:0008629Pulsatile tinnitus1SDHAF2 CL E G H5494926034OMIM:601650Paragangliomas 2.55
HP:0000360HP:0008629Pulsatile tinnitus1SDHB CL E G H639010681ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent237
HP:0000360HP:0008629Pulsatile tinnitus1SDHB CL E G H639010681OMIM:115310Paragangliomas 4.237
HP:0000360HP:0008629Pulsatile tinnitus1SDHB CL E G H639010681ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent237
HP:0000360HP:0008629Pulsatile tinnitus1SDHC CL E G H639110682ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent147
HP:0000360HP:0008629Pulsatile tinnitus1SDHC CL E G H639110682OMIM:605373Paragangliomas 3.147
HP:0000360HP:0008629Pulsatile tinnitus1SDHD CL E G H639210683ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent129
HP:0000360HP:0008629Pulsatile tinnitus1SDHD CL E G H639210683OMIM:168000Paragangliomas 1.129
HP:0000360HP:0008629Pulsatile tinnitus1SDHD CL E G H639210683ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent129
HP:0000360HP:0008629Pulsatile tinnitus1SLC25A11 CL E G H840210981ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent
HP:0000360HP:0008629Pulsatile tinnitus1TMEM127 CL E G H5565426038ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent131
HP:0000360HP:0008629Pulsatile tinnitus1VHL CL E G H742812687ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040282 - Frequent490
HP:0000360HP:0008629Pulsatile tinnitus1VHL CL E G H742812687ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040282 - Frequent490


Genes (61) :AIFM1 AKT1 ATP1A2 ATP2B2 BAP1 CACNA1A CACNA1D CAV1 CCND1 CLCN2 CLCNKB COCH CYP11B1 CYP11B2 DIABLO DKK1 DLST DNMT3A DSPP EPAS1 FH GRM1 JAK2 KCNJ5 KCNQ4 KIF1B MAX MDH2 MFN2 MIR96 MPL NAGA NF1 NF2 OSBPL2 P2RX2 PDGFB PIK3CA PMP22 PRRT2 RET SCN1A SDHA SDHAF2 SDHB SDHC SDHD SLC12A3 SLC25A11 SLC39A14 SLC44A4 SMARCB1 SMARCE1 SMO SUFU TERT TET2 TMC1 TMEM127 TRAF7 VHL

Diseases (38) :OMIM:300614 ORPHA:2495 ORPHA:569 OMIM:619804 OMIM:108500 ORPHA:97 ORPHA:369929 OMIM:606721 OMIM:193300 ORPHA:404 ORPHA:358 OMIM:601369 ORPHA:403 OMIM:614152 ORPHA:268882 ORPHA:29072 ORPHA:276621 OMIM:605594 OMIM:617691 ORPHA:729 ORPHA:251274 OMIM:600101 OMIM:601152 OMIM:613074 ORPHA:79280 ORPHA:637 OMIM:101000 OMIM:616340 OMIM:608224 ORPHA:90658 OMIM:601650 ORPHA:97286 OMIM:115310 OMIM:605373 OMIM:168000 OMIM:144755 OMIM:617606 OMIM:606705
 

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