raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:519282

Rare corneal disorder

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare corneal disorder
frMaladie cornéenne rare
deSeltene Krankheit der Cornea
esTrastorno corneal raro
itPatologia corneale rara
nlZeldzame aandoening van corneaZeldzame aandoening van hoornvlies
ptDoença rara da córnea
plRzadka choroba rogówki
csVzácná porucha rohovky
ukРідкісне захворювання рогівки
zh罕见角膜病变
trNadir kornea bozukluğu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681393Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (4):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card