C176823Level 9
MHC Class II Deficiency
**Semantic type:** Disease or Syndrome
**Definition:** A genetic disorder caused by molecular defects in the genes encoding for four regulatory factors controlling transcription of MHC class II genes. The phenotype is similar to SCID, and susceptibility to infection by viral, bacterial, fungal and protozoal agents is characteristic of the disease.
**Synonyms:** - MHC class II deficiency
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