DISEASES

Disease-gene associations mined from literature

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Human genes for PEHO syndrome

PEHO syndrome [DOID:0080539]

A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss.

Synonyms:  PEHO syndrome,  DOID:0080539,  PEHO disease,  PEHO disorder,  PEHO syndromes

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.