Description
otosclerosis: Formation of spongy bone in the labyrinth capsule which can progress toward the stapes (stapedial fixation) or anteriorly toward the cochlea leading to conductive, sensorineural, or mixed hearing loss. Several genes are associated with familial otosclerosis with varied clinical signs.
Data source
FinnGen phenocode |
H8_OTOSCLE |
Hospital Discharge registry |
ICD-10: H80, ICD-9: 387, ICD-8: 38699 |
Cause of Death registry |
ICD-10: H80, ICD-9: 387, ICD-8: 38699 |
Level in the ICD-hierarchy |
3 |
First defined in version |
DF2 |
Ontology