raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:423998

Rare epithelial tumor of rectum

Synonyms: Rare rectal epithelial tumor

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 epithelial tumor of rectumRare rectal epithelial tumor
frTumeur épithéliale rare du rectumTumeur épithéliale rectale rare
deSeltener epithelialer Tumor des RektumsSeltener epithelialer Tumor des Mastdarms
esTumor epitelial raro de rectoTumor rectal epitelial raro
itTumore epiteliale raro del rettoTumore epiteliale rettale raro
nlZeldzame epitheliale tumor van rectumZeldzame rectale epitheliale tumor
ptTumor epitelial maligno raro do reto
plRzadki nabłonkowy guz odbytu= en
csVzácný epiteliální tumor rektaVzácný rektální epiteliální nádor
ukРідкісна епітеліальна пухлина прямої кишкиРідкісна епітеліальна пухлина прямої кишки
zh罕见直肠上皮肿瘤罕见直肠上皮肿瘤
trNadir rektum epitel tümörüNadir rektal epitel tümör
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18514Evalidated
UMLSC5680074Evalidated

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 (2):

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