MHC Class II Deficiency

Preferred Label : MHC Class II Deficiency;

NCIt 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.;

NCI Metathesaurus CUI : CL1642592;

Détails

Origin ID

C176823;

UMLS CUI

C5447452;

Currated CISMeF NLP mapping
- Immunodeficiency by defective expression of MHC class II [ORDO Disease]
- MHC class II deficiency [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
disease_has_primary_anatomic_site
- Immune System [NCIt concept]
disease_may_have_associated_disease
- Lymphoproliferative Disease Associated with Primary Immune Disorder [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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