Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandHearing Disorders (D006311)
..Starting node
..expandTinnitus (D014012)

       Child Nodes:
........expandEpisodic Ataxia, Type 3 (C564697)



 Sister Nodes: 
..expandCongenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia (C580009)
..expandHearing Loss (D034381) Child397
..expandHyperacusis (D012001)
..expandOssicular Malformations, familial (C537142)
..expandTinnitus (D014012) Child1
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:11108
Name:Tinnitus
Definition:A nonspecific symptom of hearing disorder characterized by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear. Objective tinnitus refers to noises generated from within the ear or adjacent structures that can be heard by other individuals. The term subjective tinnitus is used when the sound is audible only to the affected individual. Tinnitus may occur as a manifestation of COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; and other conditions.
Alternative IDs:
ParentIDs:MESH:D006311
TreeNumbers:C09.218.458.670 |C10.597.751.418.670 |C23.888.592.763.393.670
Synonyms:Clicking Tinnitus |Induced Tinnitus, Noise |Leudet's Tinnitus |Leudet Tinnitus |Noise Induced Tinnitus |Objective Tinnitus |Pulsatile Tinnitus |Ringing Buzzing Tinnitus |Ringing-Buzzing-Tinnitus |Spontaneous Oto Acoustic Emission Tinnitus |Spontaneous Oto-Acoustic
Slim Mappings:Ear-nose-throat disease|Nervous system disease|Signs and symptoms
Reference: MedGen: D014012
MeSH: D014012
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants