agammaglobulinemia, Non-Bruton type, autosomal dominant

Preferred Label : agammaglobulinemia, Non-Bruton type, autosomal dominant;

MeSH note : this form caused by mutation in mu immunoglobulin heavy-chain gene;

Details

Origin ID

C563305;

UMLS CUI

C3502007;

MeSH term(s) associated for indexing
- agammaglobulinemia [MeSH Descriptor]
Record concept(s)
- agammaglobulinemia, Non-Bruton type, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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