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. [ MESH : D010040 ]

Synonyms:

otosclerosis

otosclerosis (disease)

otospongiosis

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:387.8 (MONDO:relatedTo)
  • MESH:D010040 (MONDO:equivalentTo)
  • HP:0000362 (MONDO:otherHierarchy)
  • SCTID:11543004 (MONDO:equivalentTo)
  • ICD10:H80
  • MedDRA:10033103
  • UMLS:C0029899 (MONDO:equivalentTo)
  • DOID:12185 (MONDO:equivalentTo)
  • MedDRA:10033108
  • ICD9:387.9 (MONDO:i2s)
  • MedDRA:10033107
  • MONDO:0005349
  • ICD9:387 (EFO:0004213)
  • MeSH:D010040
  • OMIMPS:166800 (MONDO:equivalentTo)
  • SNOMEDCT:11543004
  • Orphanet:2794 (MONDO:equivalentTo)
IAO 0000589
  • otosclerosis (disease)
exactMatch
  • http://linkedlifedata.com/resource/umls/id/C0029899
  • http://purl.obolibrary.org/obo/Orphanet_2794
  • http://purl.obolibrary.org/obo/DOID_12185
  • http://identifiers.org/snomedct/11543004
  • http://identifiers.org/mesh/D010040
  • https://omim.org/phenotypicSeries/PS166800
gwas trait
  • true
id
  • EFO:0004213
term editor
  • Dani Welter