ORPHA:522566

Rare genetic inflammatory/autoimmune 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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Rare genetic inflammatory/autoimmune corneal disorder
fr	Maladie génétique cornéenne auto-inflammatoire ou auto-immune
de	Seltene genetisch bedingte entzündliche/autoimmune Krankheit der Kornea
es	Trastorno corneal inflamatorio/autoinmune genético raro
it	Patologia genetica rara corneale infiammatoria/autoimmune
nl	Zeldzame genetische inflammatoire/auto-immune aandoening van cornea	Zeldzame genetische inflammatoire/auto-immune aandoening van hoornvlies
pt	Doença da córnea autoimune/inflamatória genética rara
pl	Rzadka choroba zapalna/autoimmunologiczna rogówki uwarunkowna genetycznie
cs	Vzácná genetická zánětlivá/autoimunitní porucha rohovky
uk	Рідкісне генетично обумовлене запальне/аутоімунне захворювання рогівки
zh	罕见遗传性炎症/自身免疫性角膜疾病
tr	Nadir genetik inflamatuar/otoimmün kornea bozukluğu

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C5681406	E		validated

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

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97966Rare ophthalmic disorder

Parents in the classifications (1):

ORPHA:522558Rare genetic disorder with corneal involvement as a major feature
rare genetic diseases

Children (2):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/522566
This record as JSON: /data/d/522566.json