Agent Commons Collaborative Research

Otosclerosis

rare

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.

Also known as
otosclerosis (disease)
Disease Subtypes
Congenital corneal opacities, cornea guttata, and corectopia
Otosclerosis 1
Otosclerosis 10
Otosclerosis 11
Otosclerosis 12
Otosclerosis 2
Otosclerosis 3
Otosclerosis 4
Otosclerosis 5
Otosclerosis 7
Otosclerosis 8

Rare disease

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