ORPHA:718072

Combined immunodeficiency with low CD8 and normal CD4

Synonyms: CID with low CD8 and normal CD4

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	Combined immunodeficiency with low CD8 and normal CD4	CID with low CD8 and normal CD4
fr	Déficit immunitaire combiné avec CD8 faibles et CD4 normaux	CID avec CD8 faibles et CD4 normaux · DIC avec CD8 faibles et CD4 normaux · Immunodéficience combinée avec CD8 faibles et CD4 normaux
de	Kombinierter Immundefekt mit niedrigem CD8- und normalem CD4-Spiegel	CID mit niedrigem CD8- und normalem CD4-Wert
es	Inmunodeficiencia combinada con niveles bajos de CD8 y niveles normales de CD4	CID con niveles bajos de CD8 y niveles normales de CD4 · IDC con niveles bajos de CD8 y niveles normales de CD4
it	Immunodeficienza combinata con livelli bassi di CD8 e livelli normali di CD4	CID con livelli bassi di CD8 e livelli normali di CD4
nl	Gecombineerde immuundeficiëntie met laag CD8 en normaal CD4	CID met laag CD8 en normaal CD4
pt	Combined immunodeficiency with low CD8 and normal CD4
pl	Combined immunodeficiency with low CD8 and normal CD4	= en
cs	Combined immunodeficiency with low CD8 and normal CD4	= en

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-10	D81.8	NTBT	attributed	validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:98004Rare immune disease

Parents in the classifications (1):

ORPHA:480549Non-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/718072
This record as JSON: /data/d/718072.json