DISEASES

Disease-gene associations mined from literature

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Human genes for autoimmune lymphoproliferative syndrome type 3

Autoimmune lymphoproliferative syndrome type 3 [DOID:0110119]

An autoimmune lymphoproliferative syndrome that has_material_basis_in homozygous mutation in the PRKCD gene on chromosome 3p21.

Synonyms:  autoimmune lymphoproliferative syndrome type 3,  DOID:0110119,  ALPS3,  autoimmune lymphoproliferative syndrome type III,  common variable immunodeficiency 9 ...

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.