DISEASES

Disease-gene associations mined from literature

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Human genes for intestinal hypomagnesemia 1

Intestinal hypomagnesemia 1 [DOID:0060883]

A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorbtion and kidney excretion and secondary hypocalcemia that has material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21.

Synonyms:  intestinal hypomagnesemia 1,  DOID:0060883,  HOMG1,  hypomagnesemia caused by selective magnesium malabsorption,  hypomagnesemia intestinal type 1 ...

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.