raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:231205

Common variable immunodeficiency without known genetic defect

Synonyms: CVID without known genetic defect

Type
Disease
Group
Disorder
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enCommon variable immunodeficiency without known genetic defectCVID without known genetic defect
frDéficit immunitaire commun variable sans défaut génétique connuCVID sans anomalie génétique connue · CVID sans défaut génétique connu · DICV sans défaut génétique connu · Immunodéficience commune variable sans défaut génétique connu
deImmundefekt, allgemeiner variabler, ohne genetischen DefektCVID ohne bekannten genetischen Defekt
esInmunodeficiencia común variable sin anomalía genética conocidaIDCV sin anomalía genética conocida
itImmunodeficienza variabile comune senza difetto genetico noto
nlGewone variabele immuundeficiëntie zonder bekend genetisch defectCVID zonder bekend genetisch defect
ptImunodeficiência variável comum sem anomalia genética conhecidaCVID sem anomalia genética conhecida
plPospolity zmienny Niedobór odpornosci bez znanego bledu genetycznego= en
csBěžná variabilní imunodeficience bez známé genetické vady= en
ukЗАСТАРІЛО: Загальний варіабельний імунодефіцит без відомого генетичного дефекту
zh弃用:普通可变性免疫缺陷不伴已知基因缺陷
trEski adı: Bilinen genetik defekt olmayan yaygın değişken immün yetmezlik
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

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