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Summary Literature (0)
DOID:0111398 - congenital dyserythropoietic anemia type Ia


Disease Ontology 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.

Synonyms: CDA Ia, CDAN1A,

Xenbase Genes : cdan1



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), congenital dyserythropoietic anemia type I (is_a)