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 IIIa ID (Ontology) DOID:0111399 (Human Disease)
Definition A congenital dyserythropoietic anemia characterized by nonprogressive mild to moderate hemolytic anemia, macrocytosis in the peripheral blood, intravascular hemolysis, and giant multinucleated erythroblasts in the bone marrow and that has_material_basis_in heterozygous mutation in the KIF23 gene on chromosome 15q23.
Also Known As "anaemia with multinucleated erythroblasts" ; "anemia with multinucleated erythroblasts" ; "CDA III" (for all, see Synonyms field below)
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 Genes
 congenital dyserythropoietic anemia type IIIa       1
 for disease ribbon | congenital dyserythropoietic anemia type IIIa       1
 model of | congenital dyserythropoietic anemia type IIIa       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease___________
congenital hemolytic anemia              |
 |__congenital dyserythropoietic anemia__|
                                         congenital dyserythropoietic anemia type IIIa  1 rec.
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Is a autosomal dominant disease
congenital dyserythropoietic anemia
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Synonyms
  • "anaemia with multinucleated erythroblasts" EXACT
    "anemia with multinucleated erythroblasts" EXACT
    "CDA III" EXACT OMO:0003012
    "CDA type 3" EXACT
    "CDA type III" EXACT
    "CDAN3" EXACT OMO:0003012
    "Congenital dyserythropoietic anaemia type 3" EXACT
    "congenital dyserythropoietic anaemia type III" EXACT
    "Congenital dyserythropoietic anemia type 3" EXACT
    "hereditary benign erythroreticulosis" EXACT
Secondary IDs
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GARD:2002
MIM:105600
ORDO:98870
SNOMEDCT_US_2023_03_01:26409005
UMLS_CUI:C0271934