raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98364

Rare constitutional hemolytic anemia due to a red cell membrane anomaly

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 hemolytic anemia due to a red cell membrane anomaly
frAnémie hémolytique constitutionnelle rare par anomalie de la membrane du globule rouge
deSeltene konstitutionelle hämolytische Anämie durch Membrananomalie der roten Blutkörperchen
esAnemia hemolítica constitucional rara por una anomalía de la membrana eritrocitaria
itAnemia emolitica costituzionale rara da anomalie della membrana dei globuli rossi
nlZeldzame constitutionele hemolytische anemie als gevolg van een rode celmembraananomalie
ptAnemia por anomalia da membrana dos glóbulos vermelhos
plRzadka niedokrwistość hemolityczna konstytucjonalna z powodu anomalii błony komórkowej czerwonych krwinek
csVzácné konstituční hemolytické anémie způsobené anomáliemi membrány červených krvinek
ukРідкісна конституціональна гемолітична анемія через аномалію еритроцитарної мембрани
zh红细胞膜异常所致罕见原发性溶血性贫血
trKırmızı hücre zarı anomalisine bağlı nadir yapısal hemolitik anemi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681716Evalidated

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