raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:180303

Rare non-malformative uterine adnexal disease

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 non-malformative uterine adnexal disease
frMaladie rare non malformative des annexes utérines
deSeltene Krankheit des Uterus und der Adnexen, nicht-malformativ
esEnfermedad rara no malformativa de los anexos uterinos
itMalattia annessiale uterina non malformativa rara
nlZeldzame niet-malformatieve uteriene adnexale ziekte
ptDoença dos anexos uterinos, rara
plRzadka choroba przydatków macicy bez malformacji
csVzácné nemalformující nemoci děložních adnex
ukРідкісне не мальформативне захворювання придатків матки
zh罕见非畸形的子宫附件疾病
trNadir görülen malformatif uterin adneksiyal hastalık
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15875Evalidated
UMLSC5681841Evalidated

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):

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