dystrophies primarily involving the retinal pigment epithelium

Go to external page http://purl.obolibrary.org/obo/MONDO_0001924


This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0154865 (MONDO:equivalentTo)
  • ICD10CM:H35.54 (MONDO:equivalentTo)
  • DOID:14252 (MONDO:equivalentTo)
  • ICD9:362.76 (MONDO:relatedTo)
  • MEDGEN:1843460 (MONDO:equivalentTo)
  • icd11.foundation:1387676300 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, mondo_top_grouping_disorder_of_visual_system, matrix_llm__txgnn_other, mondo_top_grouping_member, harrisons_view_psychiatric_disorder, matrix_included, matrix_txgnn_grouping_member, rare, matrix_txgnn_grouping_psychiatric_disorder, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, harrisons_view_disorder_of_visual_system, matrix_llm__tag_existing_treatment_other, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, icd10_billable, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_orbital_region

exactMatch

http://purl.obolibrary.org/obo/DOID_14252

http://purl.bioontology.org/ontology/ICD10CM/H35.54

http://linkedlifedata.com/resource/umls/id/C0154865

http://identifiers.org/medgen/1843460

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1387676300

id

MONDO:0001924