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otosclerosis
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description 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.
Disease Ontology Description An otitis interna characterized by an abnormal bone growth in the middle ear.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
COHD:439035
DOID:12185
EFO:0004213
ICD9:387.9
MESH:D010040
OMIMPS:166800
SCTID:11543004
UMLS:C0029899
MONDO:0005349
High level summary of knowledge for a disease, including descriptions and datasource references.