ORPHA:101978

OBSOLETE: Disease with severe reduction in all serum immunoglobulin isotypes with profoundly decreased or absent B cells

inactive · referred to ORPHA:101977Immunodeficiency due to predominantly antibodies defect

Type: Category
Group: Group of disorders
Status: inactive
Flag: Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Immunodeficiency predominantly affecting antibody production

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Disease with severe reduction in all serum immunoglobulin isotypes with profoundly decreased or absent B cells
fr	OBSOLETE : Maladie avec diminution importante d'immunoglobulines sériques et diminution ou absence de cellules B
de	OBSOLET: Krankheit mit schwerer Reduktion der Serum-Immunglobuline aller Isotypen und deutlich reduzierten oder fehlenden B-Zellen
es	OBSOLETO: Enfermedad con reducción grave de los isotipos de inmonoglobulinas séricas y con ausencia o disminución profunda de células B
it	OBSOLETO: Agammaglobulinemia
nl	OBSOLEET: Ziekte met ernstige vermindering van alle serumimmunoglobuline-isotypes met sterk verminderde of afwezige B-cellen
pt	OBSOLETO: Doença com redução grave de todas os isotipos de imunoglobulinas séricas e com ausência ou diminuição acentuada de células B
pl	NIEAKTUALNE: Choroba ze znacznym niedoborem wszystkich izotypów immunoglobulin osocza z glebokim obnizeniem lub brakiem komórek B
cs	NEAKTUÁLNÍ: Onemocnění se závažným snížením všech izotypů sérových imunoglobulinů s hluboce sníženými nebo chybějícími B-buňkami
uk	ЗАСТАРІЛО: Захворювання з вираженим зниженням усіх ізотипів імуноглобулінів у сироватці крові з глибоким зниженням або відсутністю В-лімфоцитів
zh	弃用：所有血清同型免疫球蛋白严重减少和B细胞显著减少或缺失的疾病
tr	Eski adı: B hücrelerinin tamamen azaldığı veya olmadığı tüm serum immünoglobulin izotiplerinde ağır azalma ile seyreden hastalık

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/101978
This record as JSON: /data/d/101978.json