cholesteatoma
A pathologic process characterized by the proliferation of keratinizing squamous epithelium resulting in the accumulation of keratin and cells in the middle ear and/or mastoid. It may be congenital or acquired. If left untreated, it may increase in size and destroy adjacent structures. [ NCIT:P378 ]
Term info
- GARD:0010422 (MONDO:shared-umls-xref)
- NCIT:C2944 (MONDO:equivalentTo)
- HP:0009797 (MONDO:otherHierarchy)
- ICD9:385.30 (MONDO:i2s)
- EFO:1000675 (MONDO:equivalentTo)
- SCTID:363668000 (MONDO:equivalentTo)
- DOID:869 (MONDO:equivalentTo)
- MESH:D002781 (MONDO:equivalentTo)
- UMLS:C0008373 (NCIT:C2944)
cholesteatoma (disease)
A pathologic process characterized by the proliferation of keratinizing squamous epithelium resulting in the accumulation of keratin and cells in the middle ear and/or mastoid. It may be congenital or acquired. If left untreated, it may increase in size and destroy adjacent structures.
http://purl.obolibrary.org/obo/DOID_869, http://linkedlifedata.com/resource/umls/id/C0008373, http://purl.obolibrary.org/obo/NCIT_C2944, http://identifiers.org/mesh/D002781, http://identifiers.org/snomedct/363668000
cholesteatoma, cholesteatoma (disease)
congenital cholesteatoma (type), secondary acquired cholesteatoma (type), primary acquired cholesteatoma (type)
MONDO:0006530