raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:459348

Immunodeficiency due to a complement regulatory deficiency

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
enImmunodeficiency due to a complement regulatory deficiency
frDéficit immunitaire par déficit d'une protéine régulatrice de la cascade du complémentImmunodéficience due à un déficit d'une protéine régulatrice de la cascade du complément
deImmundefekt durch regulatorischen Proteinen-Mangel des Komplementsystems
esInmunodeficiencia por una deficiencia reguladora del complemento
itImmunodeficienza da deficit della proteina regolatrice del complemento
nlImmuundeficiëntie door deficiëntie van een regulatorische component van complementsysteem
ptImunodeficiência por deficiência da regulação do complemento
plNiedobór odporności spowodowany deficytem regulacji układu dopełniacza
csImunodeficit způsobený deficitem regulátorů komplementu
ukІмунодефіцит, зумовлений дефіцитом регуляторного комплементу
zh补体调节缺陷引起的免疫缺陷病
trKompleman düzenleyici eksikliğe bağlı immün yetmezlik
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18727Evalidated
UMLSC5681111Evalidated

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