raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:522570

Rare genetic disorder of the posterior segment of the eye

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 genetic disorder of the posterior segment of the eye
frMaladie génétique rare du segment postérieur de l'oeil
deSeltene genetische Krankheit des hinteren Augensegments
esTrastorno genético raro del segmento posterior del ojo
itMalattia genetica rara del segmento posteriore dell'occhio
nlZeldzame genetische aandoening van achterste oogsegment
ptDoença genética rara do segmento posterior do olho
plRzadka choroba tylnego odcinka oka uwarunkowana genetycznie
csVzácná genetická porucha zadního segmentu oka
ukРідкісне генетично обумовлене захворювання заднього відділу ока
zh罕见眼后节遗传性疾病
trGözün posterior segmentinde nadir görülen genetik bozukluğu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681408Evalidated

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 (1):

Codes that Orphanet moved or referred to this one:

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