raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:99974

OBSOLETE: TACI-related selective deficiency of IgA

inactive · referred to ORPHA:696907Common variable immunodeficiency phenotype due to homozygous TACI deficiency

Type
Clinical 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 phenotype due to homozygous TACI deficiency

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: TACI-related selective deficiency of IgA
frOBSOLETE : Déficit sélectif en IgA lié au gne TACI
deOBSOLET: IgA-Mangel, selektiver, TACI-abhängiger
esOBSOLETO: Deficiencia selectiva de IgA asociada a TACI
itOBSOLETO: Deficit selettivo di IgA TACI-associato
nlOBSOLEET: TACI-gerelateerde selectieve deficiëntie van IgA
ptOBSOLETO: Deficiência seletiva de IgA TACI-relacionada
plNIEAKTUALNE: Selektywny Niedobór IgA zwiazany z TACI
csNEAKTUÁLNÍ: Selektivní deficit IgA související s TACI
ukЗАСТАРІЛО: Селективний дефіцит IgA, повязаний з TACI
zh弃用:TACI相关IgA选择性缺乏
trEski adı: TACI -ilişkili selektif IgA eksikliği
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

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