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:C0010036 (E (Exact mapping: the two concepts are equivalent))
  • 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).)
  • 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