Search Ontology:
Human Disease

congenital dyserythropoietic anemia type Ia

Term ID
DOID:0111398
Synonyms
  • CDA Ia
  • CDAN1A
Definition
A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in the CDAN1 gene on chromosome 15q15.2. https://www.ncbi.nlm.nih.gov/pubmed/12434312
References
Ontology
Human Disease   ( DOID:0111398 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations