raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98360

Constitutional anemia due to iron metabolism disorder

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
enConstitutional anemia due to iron metabolism disorder
frAnémie constitutionnelle due à une anomalie du métabolisme du fer
deKonstitutionelle Anämie durch Störung des Eisenstoffwechsels
esAnemia constitucional por trastorno del metabolismo del hierro
itAnemia costituzionale da anomalie del metabolismo del ferro
nlConstitutionele anemie als gevolg van een ijzerstofwisselingsstoornis
ptDoença do metabolismo do ferro e da síntese do heme
plNiedokrwistość konstytucjonalna z powodu zaburzenia metabolizmu żelaza
csKonstituční anémie způsobená poruchou metabolismu železa
ukКонституційна анемія внаслідок порушення обміну заліза
zh铁代谢异常所致造血成分相关性贫血
trDemir metabolizması bozukluğuna bağlı yapısal anemi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681718Evalidated

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 (5):

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