ORPHA:77303

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

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

Synonyms: OBSOLETE: CVID due to an intrinsic B 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 B cell defect	OBSOLETE: CVID due to an intrinsic B cell defect
fr	OBSOLETE : Déficit immunitaire commun variable dé à un défaut intrinsque des cellules B	OBSOLETE : CVID dû à un défaut intrinsèque des cellules B
de	OBSOLET: Immundefekt, allgemeiner variabler, durch intrinsischen B-Zell-Defekt	OBSOLET: CVID durch intrinsischen B-Zell-Defekt
es	OBSOLETO: Inmunodeficiencia común variable por defecto intrínseco de las células B	OBSOLETO: IDCV por defecto intrínseco de células B
it	OBSOLETO: Immunodeficienza variabile comune da difetto intrinseco delle cellule B	OBSOLETO: CVID da difetto intrinseco delle cellule B
nl	OBSOLEET: Algemene variabele immuundeficiëntie als gevolg van een intrinsiek B cel-defect	OBSOLEET: CVID als gevolg van een intrinsiek B cel-defect
pt	OBSOLETO: Hipogamaglobulinemia por deficiência de CD19
pl	NIEAKTUALNE: Powszechny zmienny Niedobór odpornosci z powodu wewnetrznego defektu komórek B	NIEAKTUALNE: CVID z powodu wewnętrznego defektu komórek B
cs	NEAKTUÁLNÍ: Common variable immunodeficiency due to an intrinsic B cell defect	= en
uk	ЗАСТАРІЛО: Простий варіабельний імунодефіцит, зумовлений вродженим дефектом В-клітин	ЗАСТАРІЛО: CVID внаслідок вродженого дефекту В-клітин
zh	弃用：内在B细胞缺陷所致常见变异型免疫缺陷病	固有B细胞缺陷所致CVID
tr	Eski adı: İntrinsik B hücresi defektine bağlı yaygın değişken immün yetmezlik	İntrinsik bir B 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/77303
This record as JSON: /data/d/77303.json