DISEASES

Disease-gene associations mined from literature

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Human genes for autoimmune lymphoproliferative syndrome type 2B

Autoimmune lymphoproliferative syndrome type 2B [DOID:0110116]

An autoimmune lymphoproliferative syndrome that has_material_basis_in homozygous mutation in the CASP8 gene on chromosome 2q33.

Synonyms:  autoimmune lymphoproliferative syndrome type 2B,  DOID:0110116,  ALPS2B,  ALPS with recurrent viral infections,  autoimmune lymphoproliferative syndrome type IIB ...

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.