raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2284

OBSOLETE: Primary T cell immunodeficiency

inactive · referred to ORPHA:179006Primary immunodeficiency due to a defect in adaptive immunity

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Primary immunodeficiency due to a defect in adaptive immunity

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Primary T cell immunodeficiency
frOBSOLETE : Immunodéficience primitive en cellules T
deOBSOLET: T-Zell-Immundefekt, primäre Form
esOBSOLETO: Immunodeficiencia primaria de células T
itOBSOLETO: Immunodeficienza primitiva delle cellule T
nlOBSOLEET: Primaire T-cel-immuundeficiëntie
ptOBSOLETO: Imunodeficiência de células T primária
plNIEAKTUALNE: Pierwotny Niedobór odpornosci zalezny od komórek T
csNEAKTUÁLNÍ: Primární T buněčná imunodeficience
ukЗАСТАРІЛО: Первинний Т-клітинний імунодефіцит
zh弃用:原发性T细胞免疫缺陷病
trEski adı: Primer T hücresi immün yetmezliği
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