raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:720308

T-B-NK+ severe combined immunodeficiency with microcephaly

Synonyms: T-B-NK+ SCID with microcephaly

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.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enT-B-NK+ severe combined immunodeficiency with microcephalyT-B-NK+ SCID with microcephaly
frDéficit immunitaire combiné sévère T-B-NK+ avec microcéphalieDICS T-B-NK+ avec microcéphalie · Immunodéficience combinée sévère T-B-NK+ avec microcéphalie
deImmundefekt, kombinierter schwerer, T-B-NK+, mit MikrozephalieT-B-NK+ SCID mit Mikrozephalie
esInmunodeficiencia combinada grave T-B-NK+ con microcefaliaIDCG T-B-NK+ con microcefalia · SCID T-B-NK+ con microcefalia
itImmunodeficienza combinata grave T-B-NK+ con microcefaliaSCID T-B-NK+ con microcefalia
nlT-B-NK+ ernstige gecombineerde immuundeficiëntie met microcefalieT-B-NK+ SCID met microcefalie · T-cel negatieve B-cel negatieve NK-cel positieve ernstige gecombineerde immuundeficiëntie met microcefalie
ptT-B-NK+ severe combined immunodeficiency with microcephaly
plT-B-NK+ severe combined immunodeficiency with microcephaly= en
csT-B-NK+ severe combined immunodeficiency with microcephaly= en
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (3):

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