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[X] cholesteatoma

Go to external page http://purl.obolibrary.org/obo/MONDO_0006530

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 ]

Synonyms: cholesteatoma cholesteatoma (disease)

This is just here as a test because I lose it

Term information

database cross reference
  • EFO:1000675 (MONDO:equivalentTo)
  • HP:0009797 (MONDO:otherHierarchy)
  • SCTID:363668000 (MONDO:equivalentTo)
  • NCIT:C2944 (MONDO:equivalentTo)
  • UMLS:C0008373 (MONDO:equivalentTo)
  • ICD9:385.30 (MONDO:i2s)
  • DOID:869 (MONDO:equivalentTo)
  • MEDGEN:3043 (MONDO:equivalentTo)
  • MESH:D002781 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_integumentary_system_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_integumentary_system_disorder

OBO foundry unique label

cholesteatoma (disease)

exactMatch

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/medgen/3043

http://www.ebi.ac.uk/efo/EFO_1000675

http://identifiers.org/snomedct/363668000

has related synonym

congenital cholesteatoma (type)

secondary acquired cholesteatoma (type)

primary acquired cholesteatoma (type)

id

MONDO:0006530

Term relations

Subclass of: