DISEASES

Disease-gene associations mined from literature

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Human genes for autoimmune polyendocrine syndrome type 2

Autoimmune polyendocrine syndrome type 2 [DOID:0050168]

An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene." [url:http\://en.wikipedia.org/wiki/Autoimmune_polyendocrine_syndrome_type_2] {comment="sn:IEDB"}

Synonyms:  autoimmune polyendocrine syndrome type 2,  DOID:0050168,  Schmidt syndrome,  Schmidt disease,  Schmidt disorder ...

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.