ORPHA:720294

T-B-NK- severe combined immunodeficiency

Synonyms: T-B-NK- SCID

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	T-B-NK- SCID
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-	= en
es	Inmunodeficiencia combinada grave T-B-NK-	SCID T-B-NK- · IDCG T-B-NK-
it	Immunodeficienza combinata grave T-B-NK-	SCID T-B-NK-
nl	T-B-NK- ernstige gecombineerde immuundeficiëntie	T-B-NK- SCID · T-cel negatieve B-cel negatieve NK-cel negatieve ernstige gecombineerde immuundeficiëntie
pt	T-B-NK- severe combined immunodeficiency
pl	T-B-NK- severe combined immunodeficiency	= en
cs	T-B-NK- severe combined immunodeficiency	= en

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:317419T-B- severe combined immunodeficiency
rare genetic diseases; rare immunological diseases; rare transplant-related disorders

Children (3):

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/720294
This record as JSON: /data/d/720294.json