DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Galloway-Mowat syndrome

Galloway-Mowat syndrome [DOID:0080694]

A syndrome that is characterized by developmental delay, progressive microcephaly, cerebral and cerebellar atrophy with extrapyramidal involvement, and optic atrophy.

Synonyms:  Galloway-Mowat syndrome,  DOID:0080694,  GallowayMowat syndrome,  Galloway-Mowat disease,  Galloway-Mowat disorder ...

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.