FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	hyperimmunoglobulin syndrome	ID (Ontology)	DOID:2959 (Human Disease)
Definition	A B cell deficiency that is characterized by relative predominance of certain immunoglobulin subtypes and deficiencies of others.
Comment
Links to External Ontologies
	DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Spanning Tree (Parents/Children)

  primary immunodeficiency disease
   |__B cell deficiency
       |__hyperimmunoglobulin syndrome  4 rec.
           |__hyper IgE syndrome 3 rec.
           |   |__hyper IgE recurrent infection syndrome 1 1 rec.
           |   |__hyper IgE recurrent infection syndrome 2 1 rec.
           |   |__hyper IgE recurrent infection syndrome 3 1 rec.
           |   |__hyper IgE recurrent infection syndrome 4
           |__hyper IgM syndrome
           |   |__immunodeficiency with hyper IgM type 3
           |   |__immunodeficiency with hyper IgM type 5
           |   |__immunodeficiency with hyper-IgM type 2
           |   |__immunodeficiency with hyper-IgM type 4
           |   |__X-linked hyper IgM syndrome
           |__hyperimmunoglobulinemia D periodic fever syndrome 1 rec.

Spanning Tree View Settings
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Relationships
Is a	B cell deficiency
Part of
Synonyms & Secondary IDs
Synonyms

Secondary IDs

External Crossreferences & Linkouts
	NCI:C27579 UMLS_CUI:C1334069