JSON

corneal dystrophy

^ http://purl.obolibrary.org/obo/MONDO_0018102

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 ]

Term info

database cross reference
  • ICD9:371.50 (DOID:2566)
  • HP:0001131 (MONDO:otherHierarchy)
  • MESH:D003317 (Orphanet:34533/e)
  • DOID:2566 (MONDO:equivalentTo)
  • MedDRA:10011005 (Orphanet:34533/e)
  • ICD9:371.5 (DOID:2566)
  • NCIT:C34513 (MONDO:equivalentTo)
  • UMLS:C0010036 (Orphanet:34533/e)
  • SCTID:5587004 (MONDO:equivalentTo)
  • Orphanet:34533 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

IAO 0000589

corneal dystrophy (disease)

closeMatch

http://identifiers.org/meddra/10011005

comment

Editor note: NCIT distinguishes between acquired and genetic

definition

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.

exactMatch

http://purl.obolibrary.org/obo/DOID_2566, http://purl.obolibrary.org/obo/NCIT_C34513, http://identifiers.org/snomedct/5587004, http://purl.obolibrary.org/obo/Orphanet_34533, http://linkedlifedata.com/resource/umls/id/C0010036, http://identifiers.org/mesh/D003317

has exact synonym

corneal dystrophy (disease), corneal dystrophy

id

MONDO:0018102

Term relations