(Q3508735)

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Bare lymphocyte syndrome

medical condition

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2 references

Combined immunodeficiency disease associated with absence of cell-surface HLA-A and -B antigens

stated in

Defective expression of HLA class I antigens: a case of the bare lymphocyte without immunodeficiency.

subclass of

severe combined immunodeficiency

0 references

0 references

2 references

A trans-acting class II regulatory gene unlinked to the MHC controls expression of HLA class II genes

stated in

Mutation in a winged-helix DNA-binding motif causes atypical bare lymphocyte syndrome

RFX5

2 references

stated in

A trans-acting class II regulatory gene unlinked to the MHC controls expression of HLA class II genes

stated in

Mutation in a winged-helix DNA-binding motif causes atypical bare lymphocyte syndrome

RFXANK

1 reference

stated in

Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHC class II deficiency

TAP2

1 reference

stated in

Homozygous human TAP peptide transporter mutation in HLA class I deficiency

Identifiers

DiseasesDB

29570

1 reference

imported from Wikimedia project

English Wikipedia

31627

1 reference

imported from Wikimedia project

0 references

1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

2779694405

0 references

OMIM ID

604571

1 reference

imported from Wikimedia project

English Wikipedia

209920

1 reference

imported from Wikimedia project

English Wikipedia

(Q3508735)

Bare lymphocyte syndrome

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