DISEASES

Disease-gene associations mined from literature

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Human genes for Galloway-Mowat syndrome 1

Galloway-Mowat syndrome 1 [DOID:0060364]

A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the WDR73 gene on chromosome 15q25.

Synonyms:  Galloway-Mowat syndrome 1,  DOID:0060364,  GallowayMowat syndrome 1,  Galloway syndrome,  microcephaly, hiatal hernia and nephrotic syndrome ...

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.