FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term plasma protein metabolism disease ID (Ontology) DOID:2345 (Human Disease)
Definition An inherited metabolic disorder that involves plasma protein metabolism malfunction.
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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 of metabolism__
genetic disease________|
                       inherited metabolic disorder
                        |__plasma protein metabolism disease  9 rec.
                            |__alpha 1-antitrypsin deficiency 8 rec.
                            |__carboxypeptidase N deficiency 1 rec.
                            |__macroglobulinemia
                            |__monoclonal paraproteinemia
                            |__polyclonal hypergammaglobulinemia
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a inherited metabolic disorder
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
ICD9CM:273.8
SNOMEDCT_US_2023_03_01:190822009
UMLS_CUI:C0029594