FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term wild-type amyloidosis ID (Ontology) DOID:0080937 (Human Disease)
Definition An amyloidosis that is characterized by progressive instability, misfolding and formation of amloid fibrils of the transthyretin protein.
Also Known As "Age related amyloidosis" ; "ATTRwt amyloidosis" ; "Old age amyloidosis" (for all, see Synonyms field below)
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 of metabolism
 |__amyloidosis________________
thoracic disease               |
 |__heart disease______________|
cardiovascular system disease  |
 |__heart disease______________|
                               wild-type amyloidosis
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a heart disease
amyloidosis
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Age related amyloidosis" EXACT
    "ATTRwt amyloidosis" EXACT
    "Old age amyloidosis" EXACT
    "senile systemic amyloidosis" EXACT
    "wild-type ATTR amyloidosis" EXACT
    "wild-type transthyretin cardiac amyloidosis" EXACT
Secondary IDs
hide External Crossreferences & Linkouts