DISEASES

Disease-gene associations mined from literature

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Human genes for congenital dyserythropoietic anemia type Ia

Congenital dyserythropoietic anemia type Ia [DOID:0111398]

A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in CDAN1 on chromosome 15q15.2.

Synonyms:  congenital dyserythropoietic anemia type Ia,  congenital dyserythropoietic anemia type Ias,  DOID:0111398,  CDA Ia,  CDAN1A ...

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.