FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term autosomal dominant beta thalassemia ID (Ontology) DOID:0080770 (Human Disease)
Definition A beta thalassemia that has_material_basis_in one dominantly inherited mutated HBB gene and signs and symptoms of beta-thalassemia major or beta-thalassemia intermedia.
Also Known As "inclusion body beta-thalassemia"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
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
 Full annotation statements 
Relevant FlyBase reports
 Genes
 autosomal dominant beta thalassemia       1
 for disease ribbon | autosomal dominant beta thalassemia       1
 model of | autosomal dominant beta thalassemia       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
thalassemia                     |
 |__beta thalassemia____________|
                                autosomal dominant beta thalassemia  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
beta thalassemia
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "inclusion body beta-thalassemia" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MIM:603902