DISEASES

Disease-gene associations mined from literature

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Human genes for molybdenum cofactor deficiency type B

Molybdenum cofactor deficiency type B [DOID:0111163]

A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11.

Synonyms:  molybdenum cofactor deficiency type B,  DOID:0111163,  molybdenum cofactor deficiency type Bs,  combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B,  MOCODB ...

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.