Tinnitus

Symptom Information:

Symptom ID: HPO:0000360
Synonyms:
Noises in ear (finding) [Orphanet:13580]
Tinnitus (finding) [Orphanet:13580]
Ringing in ear (finding) [Orphanet:13580]
Tinnitus [Orphanet:13580]
Tinnitus [OMIM:Tinnitus]
Tinnitus [MedDRA:10043882]
Aggravated ringing in ears [MedDRA:10043882]
Ear buzzing [MedDRA:10043882]
Ear cracking [MedDRA:10043882]
Ear crackling [MedDRA:10043882]
Ear hissing [MedDRA:10043882]
Ear noises [MedDRA:10043882]
Ear ringing [MedDRA:10043882]
Ear roaring [MedDRA:10043882]
Noises in head [MedDRA:10043882]
Objective tinnitus [MedDRA:10043882]
Ringing in ears [MedDRA:10043882]
Subjective tinnitus [MedDRA:10043882]
Tinnitus aggravated [MedDRA:10043882]
Tinnitus, unspecified [MedDRA:10043882]
Worsening of tinnitus [MedDRA:10043882]
Pulsatile tinnitus [MedDRA:10043882]
Tinnitus (less common) [OMIM:Tinnitus (less common)]
Tinnitus (rare) [OMIM:Tinnitus (rare)]
Tinnitus (variable) [OMIM:Tinnitus (variable)]
Quality:
Cross references:
Orphanet:13580 "Tinnitus" [Orphanet:13580]
OMIM: "Tinnitus" [OMIM:Tinnitus]
OMIM: "Tinnitus (less common)" [OMIM:Tinnitus (less common)]
OMIM: "Tinnitus (rare)" [OMIM:Tinnitus (rare)]
OMIM: "Tinnitus (variable)" [OMIM:Tinnitus (variable)]
UMLS:C0040264 "Tinnitus" [HPO:0000360]
UMLS:C0040264 "Tinnitus" [Orphanet:13580]
Is a (Direct Parents):
HPO         Hearing abnormality
MedDRA Inner ear signs and symptoms
Orphanet Functional anomalies of the inner ear
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Hearing abnormality(HPO:0000364)
             Tinnitus(HPO:0000360)
MedDRA:
Ear and labyrinth disorders(MedDRA:10013993)
    Inner ear and VIIIth cranial nerve disorders(MedDRA:10022396)
       Inner ear signs and symptoms(MedDRA:10022398)
          Tinnitus(HPO:0000360)
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Alport syndrome (Orphanet:63)
Arachnoiditis (Orphanet:137817)
Arnold-Chiari malformation type I (Orphanet:268882)
Carney-Stratakis syndrome (Orphanet:97286)
Cogan syndrome (Orphanet:1467)
DEAFNESS, AUTOSOMAL DOMINANT 16 (OMIM:603964)
DEAFNESS, AUTOSOMAL DOMINANT 2A (OMIM:600101)
DEAFNESS, AUTOSOMAL DOMINANT 33 (OMIM:614211)
DEAFNESS, AUTOSOMAL DOMINANT 36 (OMIM:606705)
DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1 (OMIM:605594)
DEAFNESS, AUTOSOMAL DOMINANT 58 (OMIM:615654)
DEAFNESS, AUTOSOMAL DOMINANT 67 (OMIM:616340)
DEAFNESS, AUTOSOMAL DOMINANT 9 (OMIM:601369)
DEAFNESS, Y-LINKED 1 (OMIM:400043)
Deafness, autosomal dominant 41 (OMIM:608224)
Episodic ataxia type 3 (Orphanet:79135)
Episodic ataxia type 4 (Orphanet:79136)
Fabry disease (Orphanet:324)
Familial paroxysmal ataxia (Orphanet:97)
Hereditary motor and sensory neuropathy type 6 (Orphanet:90120)
Meniere disease (Orphanet:45360)
Neurofibromatosis type 2 (Orphanet:637)
Polycythemia vera (Orphanet:729)
Relapsing polychondritis (Orphanet:728)
Usher syndrome (Orphanet:886)
VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE (OMIM:193005)
Von Hippel-Lindau disease (Orphanet:892)
Wyburn-Mason syndrome (Orphanet:53719)