DISEASES

Disease-gene associations mined from literature

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Human genes for hereditary spherocytosis

Hereditary spherocytosis [DOID:12971]

A congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape.

Synonyms:  hereditary spherocytosis,  DOID:12971,  familial spherocytosis,  hereditary spherocytosises,  Congenital spherocytic hemolytic anemia ...

Linkouts:  OMIM #1 #2 #3 #4 #5

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.