FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term congenital dyserythropoietic anemia type IVa ID (Ontology) DOID:0111400 (Human Disease)
Definition A congenital dyserythropoietic anemia characterized by ineffective erythropoiesis and hemolysis resulting in anemia and abnormal erythroblast morphology that has_material_basis_in heterozygous mutation in the KLF1 gene on chromosome 19p13.13.
Also Known As "CDA due to KLF1 mutation" ; "CDA IV" ; "CDA type 4" (for all, see Synonyms field below)
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 Genes
 congenital dyserythropoietic anemia type IVa       2
 for disease ribbon | congenital dyserythropoietic anemia type IVa       2
 model of | congenital dyserythropoietic anemia type IVa       2
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease___________
congenital hemolytic anemia              |
 |__congenital dyserythropoietic anemia__|
                                         congenital dyserythropoietic anemia type IVa  2 rec.
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Is a autosomal dominant disease
congenital dyserythropoietic anemia
Part of
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Synonyms
  • "CDA due to KLF1 mutation" EXACT
    "CDA IV" EXACT OMO:0003012
    "CDA type 4" EXACT
    "CDA type IV" EXACT
    "CDAN4" EXACT OMO:0003012
    "Congenital dyserythropoietic anaemia due to KLF1 mutation" EXACT
    "Congenital dyserythropoietic anaemia type 4" EXACT
    "congenital dyserythropoietic anaemia type IV" EXACT
    "Congenital dyserythropoietic anemia due to KLF1 mutation" EXACT
    "Congenital dyserythropoietic anemia type 4" EXACT
Secondary IDs
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MIM:613673
NCI:C157148
ORDO:293825
SNOMEDCT_US_2023_03_01:719453009
UMLS_CUI:C3150926