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Summary Literature (0)
DOID:12185 - otosclerosis

Disease Ontology Definition:An otitis interna characterized by isolated endochondral bone sclerosis of the labyrinthine capsule.

Synonyms:

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005349 - otosclerosis

MIM:
MIM:166800 - OTOSCLEROSIS 1; OTSC1
MIM:605727 - OTOSCLEROSIS 2; OTSC2
MIM:608244 - OTOSCLEROSIS 3; OTSC3
MIM:608484 - CONGENITAL CORNEAL OPACITIES, CORNEA GUTTATA, AND CORECTOPIA
MIM:611571 - OTOSCLEROSIS 4; OTSC4
MIM:611572 - OTOSCLEROSIS 7; OTSC7
MIM:612096 - OTOSCLEROSIS 8; OTSC8
MIM:615589 - OTOSCLEROSIS 10; OTSC10

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), inner ear disease (is_a)