ORPHA:720287

T-B+NK- severe combined immunodeficiency

Type: Clinical group
Group: Group of disorders
Status: active

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.

Names in Orphadata languages

9 of 12 languages

Lang	Name	Synonyms
en	T-B+NK- severe combined immunodeficiency
fr	Déficit immunitaire combiné sévère T-B+NK-	DICS T-B+NK- · Immunodéficience combinée sévère T-B+NK- · SCID T-B+NK-
de	Immundefekt, kombinierter schwerer, T-B+NK-
es	Inmunodeficiencia combinada grave T-B+NK-
it	Immunodeficienza combinata grave T-B+NK-
nl	T-B+NK- ernstige gecombineerde immuundeficiëntie	T-B+NK- SCID · T-cel negatieve B-cel positieve NK-cel negatieve ernstige gecombineerde immuundeficiëntie
pt	T-B+NK- severe combined immunodeficiency
pl	T-B+NK- severe combined immunodeficiency
cs	T-B+NK- severe combined immunodeficiency

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98004Rare immune disease

Parents in the classifications (1):

ORPHA:317416T-B+ severe combined immunodeficiency
rare genetic diseases; rare immunological diseases; rare transplant-related disorders

Children (2):

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/720287
This record as JSON: /data/d/720287.json