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.

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0010035 (E (Exact mapping: the two concepts are equivalent))
  • ICD-10:H18.5 (- E (Exact mapping: the two concepts are equivalent). - Specific code (The ORPHA code has its own code in the ICD10).)
  • UMLS:C0010036 (E (Exact mapping: the two concepts are equivalent))
  • MedDRA:10011005 (E (Exact mapping: the two concepts are equivalent))
  • MeSH:D003317 (E (Exact mapping: the two concepts are equivalent))
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=34533
hasDbXref
  • MeSH:D003317
  • ICD-10:H18.5
  • UMLS:C0010035
  • MedDRA:10011005
  • UMLS:C0010036
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409950
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409929
  • http://www.orpha.net/ORDO/Orphanet_409933
  • http://www.orpha.net/ORDO/Orphanet_409932
  • http://www.orpha.net/ORDO/Orphanet_409930
  • http://www.orpha.net/ORDO/Orphanet_409941
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409981
  • http://www.orpha.net/ORDO/Orphanet_409980
notation
  • Category
  • ORPHA:34533
present in
  • http://www.orpha.net/ORDO/Orphanet_409991
  • http://www.orpha.net/ORDO/Orphanet_410225