DISEASES

Disease-gene associations mined from literature

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Human genes for Rh deficiency syndrome

Rh deficiency syndrome [DOID:0050641]

A hemolytic anemia that is characterized by deficiency of Rh antigens, has_material_basis_in homozygous or compound heterozygous mutation in the RHAG gene on chromosome 6p12.

Synonyms:  Rh deficiency syndrome,  DOID:0050641,  Rh deficiency disease,  Rh deficiency disorder,  Rh deficiency syndromes

Linkouts:  OMIM

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.