DISEASES

Disease-gene associations mined from literature

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Human genes for split hand-foot malformation 6

Split hand-foot malformation 6 [DOID:0090026]

A split-hand/foot malformation that has_material_basis_in homozygous mutation in the WNT10B gene on chromosome 12q13.

Synonyms:  split hand-foot malformation 6,  DOID:0090026,  split handfoot malformation 6,  SHFM6

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.