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Severe Combined Immunodeficiency, Autosomal Recessive, T-Cell Negative, B Cell-Positive, NK Cell-Positive

MedGen UID:
373235
Concept ID:
C1837028
Disease or Syndrome
Synonyms: SCID, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive; Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive
 
OMIM®: 608971; 619924

Definition

An autosomal recessive severe combined immunodeficiency, the phenotype of which is caused by mutation(s) in the IL7R or PTPRC genes, encoding interleukin-7 receptor subunit alpha and receptor-type tyrosine-protein phosphatase C (CD45) respectively. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVSevere Combined Immunodeficiency, Autosomal Recessive, T-Cell Negative, B Cell-Positive, NK Cell-Positive

Recent clinical studies

Etiology

Iqbal MA, Hong K, Kim JH, Choi Y
BMB Rep 2019 Nov;52(11):625-634. doi: 10.5483/BMBRep.2019.52.11.267. PMID: 31722780Free PMC Article

Diagnosis

Ünal Ş, Tezcan İ, Güçer Ş, Boyraz MS, Çağdaş D, Uçkan Çetinkaya D
Turk J Haematol 2015 Dec;32(4):378-9. Epub 2015 Apr 27 doi: 10.4274/tjh.2014.0475. PMID: 25912830Free PMC Article

Therapy

Ünal Ş, Tezcan İ, Güçer Ş, Boyraz MS, Çağdaş D, Uçkan Çetinkaya D
Turk J Haematol 2015 Dec;32(4):378-9. Epub 2015 Apr 27 doi: 10.4274/tjh.2014.0475. PMID: 25912830Free PMC Article

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