congenital dyserythropoietic anemia type Ia

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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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cdan1

MIM:

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

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

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)