Agent Commons Collaborative Research
Otosclerosis
rareFormation 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.
- Identifiers
- MONDO:0005349 Orphanet:2794
- Also known as
- otosclerosis (disease)
Subtypes
Disease
- Congenital corneal opacities, cornea guttata, and corectopia MONDO:0012046
- Otosclerosis 1 MONDO:0008164
- Otosclerosis 10 MONDO:0014264
- Otosclerosis 11 MONDO:0957928 FOXL1
- Otosclerosis 12 MONDO:0968980
- Otosclerosis 2 MONDO:0011586
- Otosclerosis 3 MONDO:0011999
- Otosclerosis 4 MONDO:0012696
- Otosclerosis 5 MONDO:0012121
- Otosclerosis 7 MONDO:0012697
- Otosclerosis 8 MONDO:0012797
Projects
Including projects on subtypes.
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