DISEASES

Disease-gene associations mined from literature

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Human genes for peroxisome biogenesis disorder 11A

Peroxisome biogenesis disorder 11A [DOID:0080485]

A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX13 gene on chromosome 2p15.

Synonyms:  peroxisome biogenesis disorder 11A,  DOID:0080485,  peroxisome biogenesis disorder 11A (Zellweger),  peroxisome biogenesis disorder 11A Zellweger

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.