DISEASES

Disease-gene associations mined from literature

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Human genes for congenital dyserythropoietic anemia

Congenital dyserythropoietic anemia [DOID:1338]

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 dyserythropoietic anemia,  congenital dyserythropoietic anemias,  DOID:1338,  congenital dyshaematopoietic anaemia,  congenital dyshaematopoietic anaemias

Linkouts:  OMIM #1 #2 #3 #4

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.