raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:280930

Systemic diseases with posterior uveitis

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
enSystemic diseases with posterior uveitis
frMaladies systémiques avec uvéite postérieure
deSystemische Krankheit mit posteriorer Uveitis
esEnfermedades sistémicas con uveítis posterior
itMalattie sistemiche con uveite posteriore
nlSystemische ziektes met posterieure uveïtis
ptDoenças sistémicas com uveíte posterior
plChoroba układowa z zapaleniem tylnego odcinka błony naczyniowej
csSystémová onemocnění se zadní uveitidou
ukСистемні захворювання із заднім увеїтом
zh全身性疾病伴后葡萄膜炎
trPosterior üveit ile seyreden sistemik hastalıklar
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO17260Evalidated
UMLSC5681022Evalidated

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 (3):

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