Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0000360 | HP:0000360 | Tinnitus | 0 | AIFM1 CL E G H | 9131 | 8768 | OMIM:300614 | Deafness, X-linked 5 | . | | | 60 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | AKT1 CL E G H | 207 | 391 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 54 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | ATP1A2 CL E G H | 477 | 800 | ORPHA:569 | Familial or sporadic hemiplegic migraine | HP:0040283 - Occasional | | | 239 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | ATP2B2 CL E G H | 491 | 815 | OMIM:619804 | DEAFNESS, AUTOSOMAL DOMINANT 82; DFNA82 | | | | 5 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | BAP1 CL E G H | 8314 | 950 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 184 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CACNA1A CL E G H | 773 | 1388 | OMIM:108500 | Episodic ataxia, type 2 | . | | | 449 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CACNA1A CL E G H | 773 | 1388 | ORPHA:569 | Familial or sporadic hemiplegic migraine | HP:0040283 - Occasional | | | 449 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CACNA1A CL E G H | 773 | 1388 | ORPHA:97 | Familial paroxysmal ataxia | HP:0040282 - Frequent | | | 449 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CACNA1D CL E G H | 776 | 1391 | ORPHA:369929 | Primary hyperaldosteronism-seizures-neurological abnormalities syndrome | HP:0040283 - Occasional | | | 51 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CAV1 CL E G H | 857 | 1527 | OMIM:606721 | Lipodystrophy, familial partial, type 7 | | | | 11 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CCND1 CL E G H | 595 | 1582 | OMIM:193300 | Von hippel-lindau syndrome | . | | | 1 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CLCN2 CL E G H | 1181 | 2020 | ORPHA:404 | Familial hyperaldosteronism type II | HP:0040283 - Occasional | | | 44 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CLCNKB CL E G H | 1188 | 2027 | ORPHA:358 | Gitelman syndrome | HP:0040284 - Very rare | | | 27 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | COCH CL E G H | 1690 | 2180 | OMIM:601369 | Deafness, autosomal dominant 9 | . | | | 46 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CYP11B1 CL E G H | 1584 | 2591 | ORPHA:403 | Familial hyperaldosteronism type I | HP:0040283 - Occasional | | | 112 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | CYP11B2 CL E G H | 1585 | 2592 | ORPHA:403 | Familial hyperaldosteronism type I | HP:0040283 - Occasional | | | 73 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | DIABLO CL E G H | 56616 | 21528 | OMIM:614152 | Deafness, autosomal dominant 64 | . | | | 11 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | DKK1 CL E G H | 22943 | 2891 | ORPHA:268882 | Arnold-Chiari malformation type I | HP:0040282 - Frequent | | | | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | DLST CL E G H | 1743 | 2911 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | DNMT3A CL E G H | 1788 | 2978 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | | | | 44 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | DSPP CL E G H | 1834 | 3054 | OMIM:605594 | Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 | . | | | 38 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | EPAS1 CL E G H | 2034 | 3374 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | | | | 112 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | FH CL E G H | 2271 | 3700 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 301 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | GRM1 CL E G H | 2911 | 4593 | OMIM:617691 | SPINOCEREBELLAR ATAXIA 44; SCA44 | | | | 8 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | JAK2 CL E G H | 3717 | 6192 | ORPHA:729 | Polycythemia vera | HP:0040281 - Very frequent | | | 57 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | KCNJ5 CL E G H | 3762 | 6266 | ORPHA:251274 | Familial hyperaldosteronism type III | HP:0040283 - Occasional | | | 128 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | KCNQ4 CL E G H | 9132 | 6298 | OMIM:600101 | Deafness, autosomal dominant nonsyndromic sensorineural 2 | . | | | 76 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | KIF1B CL E G H | 23095 | 16636 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 202 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | MAX CL E G H | 4149 | 6913 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 84 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | MDH2 CL E G H | 4191 | 6971 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 4 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | MFN2 CL E G H | 9927 | 16877 | OMIM:601152 | Hereditary motor and sensory neuropathy VI | . | | | 203 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | MIR96 CL E G H | 407053 | 31648 | OMIM:613074 | Deafness, autosomal dominant 50 | HP:0040283 - Occasional | | | 4 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | MPL CL E G H | 4352 | 7217 | ORPHA:729 | Polycythemia vera | HP:0040281 - Very frequent | | | 97 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | NAGA CL E G H | 4668 | 7631 | ORPHA:79280 | Alpha-N-acetylgalactosaminidase deficiency type 2 | HP:0040282 - Frequent | | | 47 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | NF1 CL E G H | 4763 | 7765 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 1952 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | NF2 CL E G H | 4771 | 7773 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 220 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | NF2 CL E G H | 4771 | 7773 | ORPHA:637 | Neurofibromatosis type 2 | HP:0040283 - Occasional | | | 220 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | NF2 CL E G H | 4771 | 7773 | OMIM:101000 | Neurofibromatosis, type II | | | | 220 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | OSBPL2 CL E G H | 9885 | 15761 | OMIM:616340 | DEAFNESS, AUTOSOMAL DOMINANT 67; DFNA67 | | | | 2 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | P2RX2 CL E G H | 22953 | 15459 | OMIM:608224 | Deafness, autosomal dominant 41 | . | | | 23 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | PDGFB CL E G H | 5155 | 8800 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 9 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 162 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | PMP22 CL E G H | 5376 | 9118 | ORPHA:90658 | Charcot-Marie-Tooth disease type 1E | HP:0040283 - Occasional | | | 79 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | PRRT2 CL E G H | 112476 | 30500 | ORPHA:569 | Familial or sporadic hemiplegic migraine | HP:0040283 - Occasional | | | 94 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | RET CL E G H | 5979 | 9967 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 572 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | RET CL E G H | 5979 | 9967 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | | | | 572 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SCN1A CL E G H | 6323 | 10585 | ORPHA:569 | Familial or sporadic hemiplegic migraine | HP:0040283 - Occasional | | | 1053 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHA CL E G H | 6389 | 10680 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 304 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHAF2 CL E G H | 54949 | 26034 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 55 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHAF2 CL E G H | 54949 | 26034 | OMIM:601650 | Paragangliomas 2 | | | | 55 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHB CL E G H | 6390 | 10681 | ORPHA:97286 | Carney-Stratakis syndrome | HP:0040282 - Frequent | | | 237 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHB CL E G H | 6390 | 10681 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 237 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHB CL E G H | 6390 | 10681 | OMIM:115310 | Paragangliomas 4 | | | | 237 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHB CL E G H | 6390 | 10681 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | | | | 237 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHC CL E G H | 6391 | 10682 | ORPHA:97286 | Carney-Stratakis syndrome | HP:0040282 - Frequent | | | 147 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHC CL E G H | 6391 | 10682 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 147 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHC CL E G H | 6391 | 10682 | OMIM:605373 | Paragangliomas 3 | | | | 147 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHD CL E G H | 6392 | 10683 | ORPHA:97286 | Carney-Stratakis syndrome | HP:0040282 - Frequent | | | 129 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHD CL E G H | 6392 | 10683 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 129 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHD CL E G H | 6392 | 10683 | OMIM:168000 | Paragangliomas 1 | | | | 129 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SDHD CL E G H | 6392 | 10683 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | | | | 129 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SLC12A3 CL E G H | 6559 | 10912 | ORPHA:358 | Gitelman syndrome | HP:0040284 - Very rare | | | 145 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SLC25A11 CL E G H | 8402 | 10981 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SLC39A14 CL E G H | 23516 | 20858 | OMIM:144755 | Hyperostosis cranialis interna | . | | | 5 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SLC44A4 CL E G H | 80736 | 13941 | OMIM:617606 | Deafness, autosomal dominant 72 | . | | | 1 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SMARCB1 CL E G H | 6598 | 11103 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 87 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SMARCE1 CL E G H | 6605 | 11109 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 47 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SMO CL E G H | 6608 | 11119 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 22 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | SUFU CL E G H | 51684 | 16466 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 124 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | TERT CL E G H | 7015 | 11730 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | 238 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | TET2 CL E G H | 54790 | 25941 | ORPHA:729 | Polycythemia vera | HP:0040281 - Very frequent | | | 3 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | TMC1 CL E G H | 117531 | 16513 | OMIM:606705 | Deafness, autosomal dominant 36 | . | | | 109 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | TMEM127 CL E G H | 55654 | 26038 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 131 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | TRAF7 CL E G H | 84231 | 20456 | ORPHA:2495 | Meningioma | HP:0040284 - Very rare | | | | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | VHL CL E G H | 7428 | 12687 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | | | | 490 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | VHL CL E G H | 7428 | 12687 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | | | | 490 | | |
HP:0000360 | HP:0000360 | Tinnitus | 0 | VHL CL E G H | 7428 | 12687 | OMIM:193300 | Von hippel-lindau syndrome | . | | | 490 | | |
HP:0000360 | HP:0034424 | Clicking tinnitus | 1 | CL E G H | | | | | | | | | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | DLST CL E G H | 1743 | 2911 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | DNMT3A CL E G H | 1788 | 2978 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | HP:0040282 - Frequent | | | 44 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | EPAS1 CL E G H | 2034 | 3374 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | HP:0040282 - Frequent | | | 112 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | FH CL E G H | 2271 | 3700 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 301 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | KIF1B CL E G H | 23095 | 16636 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 202 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | MAX CL E G H | 4149 | 6913 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 84 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | MDH2 CL E G H | 4191 | 6971 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 4 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | NF1 CL E G H | 4763 | 7765 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 1952 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | RET CL E G H | 5979 | 9967 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 572 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | RET CL E G H | 5979 | 9967 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | HP:0040282 - Frequent | | | 572 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHA CL E G H | 6389 | 10680 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 304 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHAF2 CL E G H | 54949 | 26034 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 55 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHAF2 CL E G H | 54949 | 26034 | OMIM:601650 | Paragangliomas 2 | . | | | 55 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHB CL E G H | 6390 | 10681 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 237 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHB CL E G H | 6390 | 10681 | OMIM:115310 | Paragangliomas 4 | . | | | 237 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHB CL E G H | 6390 | 10681 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | HP:0040282 - Frequent | | | 237 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHC CL E G H | 6391 | 10682 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 147 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHC CL E G H | 6391 | 10682 | OMIM:605373 | Paragangliomas 3 | . | | | 147 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHD CL E G H | 6392 | 10683 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 129 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHD CL E G H | 6392 | 10683 | OMIM:168000 | Paragangliomas 1 | . | | | 129 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SDHD CL E G H | 6392 | 10683 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | HP:0040282 - Frequent | | | 129 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | SLC25A11 CL E G H | 8402 | 10981 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | TMEM127 CL E G H | 55654 | 26038 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 131 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | VHL CL E G H | 7428 | 12687 | ORPHA:29072 | Hereditary pheochromocytoma-paraganglioma | HP:0040282 - Frequent | | | 490 | | |
HP:0000360 | HP:0008629 | Pulsatile tinnitus | 1 | VHL CL E G H | 7428 | 12687 | ORPHA:276621 | Sporadic pheochromocytoma/secreting paraganglioma | HP:0040282 - Frequent | | | 490 | | |