ORPHA:99831

OBSOLETE: Common variable immunodeficiency due to an intrinsic T cell defect

inactive · referred to ORPHA:696851Common variable immunodeficiency and related disorders

Synonyms: OBSOLETE: CVID due to an intrinsic T cell defect

Type: Etiological subtype
Group: Subtype of disorder
Status: inactive
Flag: Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Common variable immunodeficiency and related disorders

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Common variable immunodeficiency due to an intrinsic T cell defect	OBSOLETE: CVID due to an intrinsic T cell defect
fr	OBSOLETE : Déficit immunitaire commun variable dé à un défaut intrinsque des cellules T	OBSOLETE : CVID dû à un défaut intrinsèque des cellules T
de	OBSOLET: Immundefekt, allgemeiner variabler, durch intrinsischen T-Zell-Defekt	OBSOLET: CVID durch intrinsischen T-Zell-Defekt
es	OBSOLETO: Inmunodeficiencia común variable por defecto intrínseco de células T	OBSOLETO: IDCV por defecto intrínseco de células T
it	OBSOLETO: Immunodeficienza variabile comune da deficit intrinseco delle cellule T	OBSOLETO: CVID da deficit intrinseco delle cellule T
nl	OBSOLEET: Algemene variabele immuundeficiëntie door een intrinsiek T-celdefect	OBSOLEET: CVID door een intrinsiek T-celdefect
pt	OBSOLETO: Deficiência de proteína co-estimuladora induzível
pl	NIEAKTUALNE: Pospolity zmienny Niedobór odpornosci z powodu wewnetrznego defektu komórek T	NIEAKTUALNE: CVID z powodu wewnętrznego defektu komórek T
cs	NEAKTUÁLNÍ: Common variable immunodeficiency due to an intrinsic T cell defect	= en
uk	ЗАСТАРІЛО: Загальний варіабельний імунодефіцит, зумовлений вродженим дефектом Т-лімфоцитів	ЗАСТАРІЛО: CVID внаслідок вродженого дефекту Т-лімфоцитів
zh	弃用：T细胞内在缺陷所致普通变异型免疫缺陷病	先天性T细胞缺陷所致CVID
tr	Eski adı: İntrinsik bir T hücresi defekti nedeniyle yaygın değişken immün yetmezlik	İntrinsik bir T hücresi defektine bağlı CVID

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/99831
This record as JSON: /data/d/99831.json