The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise but remains in vogue because of its clinical value. [ Orphanet:34533 ]
Synonyms: corneal dystrophy (disease) corneal dystrophy
Term information
- MedDRA:10011005 (Orphanet:34533/e)
- MEDGEN:3619 (MONDO:equivalentTo)
- ICD9:371.50 (DOID:2566)
- icd11.foundation:1291475891 (https://orcid.org/0000-0001-5208-3432)
- Orphanet:34533 (MONDO:equivalentTo)
- DOID:2566 (MONDO:equivalentTo)
- UMLS:C0010036 (MONDO:equivalentTo)
- ICD9:371.5 (DOID:2566)
- MESH:D003317 (Orphanet:34533/e)
- SCTID:5587004 (MONDO:equivalentTo)
- NCIT:C34513 (MONDO:equivalentTo)
- HP:0001131 (MONDO:otherHierarchy)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, mondo_top_grouping_disorder_of_visual_system, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, harrisons_view_disorder_of_visual_system, matrix_llm__tag_existing_treatment_other, nord_rare, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, mondo_top_grouping_disorder_of_orbital_region, ordo_group_of_disorders
http://purl.obolibrary.org/obo/DOID_2566
http://purl.obolibrary.org/obo/NCIT_C34513
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1291475891
http://www.orpha.net/ORDO/Orphanet_34533
http://identifiers.org/snomedct/5587004
http://identifiers.org/medgen/3619
http://linkedlifedata.com/resource/umls/id/C0010036
http://identifiers.org/mesh/D003317