ORPHA:716435

Rare non-progressive vitreoretinopathy

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 non-progressive vitreoretinopathy
fr	Vitréorétinopathie non-progressive rare
de	Seltene nicht-progrediente Vitreoretinopathie
es	Vitreorretinopatía no progresiva rara
it	Vitreoretinopatia non progressiva rara
nl	Zeldzame niet-progressieve vitreoretinopathie
pt	Rare non-progressive vitreoretinopathy
pl	Rzadkie niepostępujące zaburzenie dotyczące głównie plamki
cs	Rare non-progressive vitreoretinopathy

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 (1):

ORPHA:98668Vitreoretinopathy
rare genetic diseases; rare ophthalmic disorders

Children (1):

ORPHA:91495Persistent hyperplastic primary vitreous

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/716435
This record as JSON: /data/d/716435.json