dystrophies primarily involving the retinal pigment epithelium
Go to external page http://purl.obolibrary.org/obo/MONDO_0001924
Term information
- 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)
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
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