FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term congenital dyserythropoietic anemia type IVb ID (Ontology) DOID:0051002 (Human Disease)
Definition A congenital dyserythropoietic anemia characterized by neonatal jaundice, hyperbilirubinemia, and severe congenital hemolytic anemia requiring transfusionn and that has_material_basis_in homozygous or compound heterozygous mutation in the KLF1 gene on chromosome 19p13.13.
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
 congenital dyserythropoietic anemia type IVb       2
 for disease ribbon | congenital dyserythropoietic anemia type IVb       2
 model of | congenital dyserythropoietic anemia type IVb       2
Spanning Tree (Parents/Children)
Only view relationship:
  congenital hemolytic anemia
   |__congenital dyserythropoietic anemia
       |__congenital dyserythropoietic anemia type IVb  2 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a congenital dyserythropoietic anemia
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
MIM:620969