raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:182040

Rare aplastic anemia

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 aplastic anemia
frAplasie médullaire rare
deAplastische Anämie, seltene
esAnemia aplásica
itAnemia aplastica rara
nlZeldzame aplastische anemie
ptAnemia aplásica rara
plAplazja szpikuRzadka anemia aplastyczna
csAplastická anémie
ukРідкісна апластична анемія
zh再生障碍性贫血
trAplastik anemi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15909Evalidated
UMLSC5816682Evalidated

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 (2):

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