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Summary Literature (0)
DOID:1338 - congenital dyserythropoietic anemia

Disease Ontology Definition:A congenital hemolytic anemia characterized by ineffective erythropoiesis, and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less than normal quantity of hemoglobin in the blood.

Synonyms: congenital dyshaematopoietic anaemia

Xenbase Genes : cdin1, sec23b, cdan1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019403 - congenital dyserythropoietic anemia

MIM:
MIM:224100 - ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE II; CDAN2
MIM:224120 - ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A
MIM:615631 - ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital hemolytic anemia (is_a)