raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:331193

Other immunodeficiency syndromes due to defects in innate immunity

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
enOther immunodeficiency syndromes due to defects in innate immunity
frAutre syndrome de déficit immunitaire par défaut de l'immunité innéeAutre syndrome d'immunodéficience par défaut de l'immunité innée
deSonstiges Immundefekt-Syndrom durch Störung der adaptiven Immunität
esOtros síndromes de inmunodeficiencia por defectos en la inmunidad innata
itAltre sindromi da immunodeficienza dovute a difetti dell'immunità innata
nlAndere immuundeficiëntiesyndromen door defecten van aangeboren immuniteit
ptOutras síndromes de imunodeficiência devidas a defeitos na imunidade inata
plInny zespół z niedoborem odporności z powodu defektów w odporności wrodzonej
csJiné syndromy imunodeficience způsobené poruchami vrozené imunity
ukІнші імунодефіцитні синдроми, зумовлені дефектами вродженого імунітету
zh先天免疫缺陷所致其他免疫缺陷综合征
trDoğumsal bağışıklık defektine bağlı diğer immün yetmezlik sendromları
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18033Evalidated
UMLSC5680945Evalidated

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 (2):

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