Tinnitus
Symptom Information:
Symptom ID: | HPO:0000360 | |||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |