DISEASES

Disease-gene associations mined from literature

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Human genes for congenital malabsorptive diarrhea 4

Congenital malabsorptive diarrhea 4 [DOID:0060779]

A congenital diarrhea characterized by chronic unremitting malabsorptive diarrhea and a profound dysgenesis of the enteroendocrine cells that has_material_basis_in mutation in the gene encoding neurogenin-3 (NEUROG3) on chromosome 10q21.3.

Synonyms:  congenital malabsorptive diarrhea 4,  DOID:0060779,  congenital malabsorptive diarrhea due to paucity of enteroendocrine cells,  congenital malabsorptive diarrhoea 4,  congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells ...

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.