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Immunodeficiency by defective expression of MHC class II

Disease definition

A rare primary genetic immunodeficiency disorder characterized by partial or complete absence of human leukocyte antigen class 2 expression resulting in severe defect in both cellular and humoral immune response to antigens. The disorder presents clinically as marked susceptibility to infections, severe malabsorption and failure to thrive and is often fatal in early childhood.

ORPHA:572

Classification level: Disorder
  • Synonym(s):
    • Bare lymphocyte syndrome type 2
    • MHC class II deficiency
  • Prevalence: Unknown
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: D81.7
  • OMIM: 209920
  • UMLS: C2931418
  • MeSH: -
  • GARD: 824
  • MedDRA: -
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