ORPHA:716198

Rare paraneoplastic choroidal 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

9 of 12 languages

Lang	Name	Synonyms
en	Rare paraneoplastic choroidal disorder
fr	Maladie choroïdienne paranéoplasique rare
de	Seltene paraneoplastische choroidale Krankheit
es	Trastorno coroideo paraneoplásico raro
it	Malattia paraneoplastica rara della coroide
nl	Zeldzame paraneoplastische aandoening van choroidea	Zeldzame paraneoplastische aandoening van vaatvlies · Zeldzame paraneoplastische choroïdale aandoening
pt	Rare paraneoplastic choroidal disorder
pl	Rzadkie paranowotworowe zaburzenie naczyniówki
cs	Rare paraneoplastic choroidal disorder

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97966Rare ophthalmic disorder

Parents in the classifications (2):

ORPHA:519309Rare choroidal disorder
rare ophthalmic disorders
ORPHA:101950Rare eye tumor
rare ophthalmic disorders; rare neoplastic diseases

Children (1):

ORPHA:674968Bilateral diffuse uveal melanocytic proliferation disease

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/716198
This record as JSON: /data/d/716198.json