JSON

[X] hereditary otorhinolaryngologic disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0018751

An instance of otorhinolaryngologic disease that is caused by a modification of the individual's genome. [ MONDO:patterns/genetic ]

Synonyms: genetic otorhinolaryngologic disease

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C5681130 (MONDO:equivalentTo)
  • Orphanet:466084 (MONDO:equivalentTo)
  • MEDGEN:1842579 (MONDO:equivalentTo)
  • GARD:21935 (MONDO:GARD)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, harrisons_view_otorhinolaryngologic_disease, matrix_excluded, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, mondo_top_grouping_otorhinolaryngologic_disease, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_hereditary_disease, ordo_group_of_disorders

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml

exactMatch

http://www.orpha.net/ORDO/Orphanet_466084

http://identifiers.org/medgen/1842579

http://linkedlifedata.com/resource/umls/id/C5681130

id

MONDO:0018751

term tracker item

https://github.com/monarch-initiative/mondo/issues/5114