raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:248302

Rare acquired deficiency 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 acquired deficiency anemia
frAnémie déficitaire acquise rare
deSeltene erworbene Mangel-Anämie
esAnemia deficitaria adquirida rara
itAnemia deficitaria acquisita rara
nlZeldzame verworven deficiëntieanemie
ptAnemia de deficiência adquirida rara
plRzadka nabyta niedokrwistość niedoborowa
csVzácné získané deficitní anémie
ukРідкісна набута дефіцитна анемія
zh罕见性获得性营养缺乏性贫血
trNadir edinsel eksiklik anemisi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16625Evalidated
UMLSC5680693Evalidated

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