Immunodeficiency, partial combined, with absence of hla determinants and beta-2-microglobulin from lymphocytes

Preferred Label : Immunodeficiency, partial combined, with absence of hla determinants and beta-2-microglobulin from lymphocytes;

Obsolete resource : true;

Moved to : 604571; 209920;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : ? Autosomal recessive;

Prefixed ID : 242870;

Details

Origin ID

242870;

UMLS CUI

C1855762;

Currated CISMeF NLP mapping
- immunodeficiency, partial combined, with absence of HLA determinants and Beta-2-Microglobulin from lymphocytes [MeSH Supplementary Concept]
- immunodeficiency, partial combined, with absence of HLA determinants and Beta-2-Microglobulin from lymphocytes [MeSH concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Decreased circulating IgG level [HPO term]
- Immunodeficiency [HPO term]
- Recurrent bacterial infections [HPO term]
- Recurrent candida infections [HPO term]
- T lymphocytopenia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- immunodeficiency, partial combined, with absence of HLA determinants and Beta-2-Microglobulin from lymphocytes [MeSH Supplementary Concept]
- immunodeficiency, partial combined, with absence of HLA determinants and Beta-2-Microglobulin from lymphocytes [MeSH concept]

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