raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:183651

Rare constitutional 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 constitutional anemia
frAnémie constitutionnelle rare
deAnämie, konstitutionelle, seltene
esAnemia constitutional rara
itAnemia costituzionale rara
nlZeldzame constitutionele anemie
ptAnemia constitucional
plRzadka anemia konstytucjonalna
csVzácné konstituční anémie
ukРідкісна конституційна анемія
zh罕见先天性贫血
trNadir yapısal anemi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15972Evalidated
UMLSC5680532Evalidated

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 (6):

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