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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.
Mondo Term and Equivalent IDs
MONDO:0005349:  otosclerosis
COHD:439035: 
EFO:0004213: 
ICD9:387.9: 
MESH:D010040: 
OMIMPS:166800: 
SCTID:11543004: 
UMLS:C0029899: