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 Ib ID (Ontology) DOID:0111397 (Human Disease)
Definition A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in the C15ORF41 gene on chromosome 15q14.
Also Known As "CDA, type Ib" ; "CDAN1B"
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 Genes
 congenital dyserythropoietic anemia type Ib       1
 for disease ribbon | congenital dyserythropoietic anemia type Ib       1
 model of | congenital dyserythropoietic anemia type Ib       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease_________________
congenital dyserythropoietic anemia             |
 |__congenital dyserythropoietic anemia type I__|
                                                congenital dyserythropoietic anemia type Ib  1 rec.
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Is a autosomal recessive disease
congenital dyserythropoietic anemia type I
Part of
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Synonyms
  • "CDA, type Ib" EXACT
    "CDAN1B" EXACT OMO:0003012
Secondary IDs
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MESH:D000742
MIM:615631
SNOMEDCT_US_2023_03_01:59548005
UMLS_CUI:C0271933