DISEASES

Disease-gene associations mined from literature

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Human genes for Muckle-Wells syndrome

Muckle-Wells syndrome [DOID:0050854]

A syndrome characterized by episodic skin rash, arthralgias, and fever associated with late-onset sensorineural deafness and renal amyloidosis that has_material_basis_in heterozygous mutation in NLRP3 on chromosome 1q44.

Synonyms:  Muckle-Wells syndrome,  DOID:0050854,  MuckleWells syndrome,  Muckle-Wells disease,  Muckle-Wells 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.