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Echinobase
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,

Echinobase Genes : cdan1


OMIM:
MIM:224120 - anemia, congenital dyserythropoietic, type ia; cdan1a

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

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