FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term congenital hypogammaglobulinemia ID (Ontology) DOID:14177 (Human Disease)
Definition
Also Known As "Congenital hypogammaglobulinaemia"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship: 
disease
 |__physical disorder_____________
primary immunodeficiency disease  |
 |__B cell deficiency_____________|
                                  congenital hypogammaglobulinemia
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a physical disorder
B cell deficiency
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Congenital hypogammaglobulinaemia" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
ICD9CM:279.04
SNOMEDCT_US_2023_03_01:190983003
UMLS_CUI:C1457897