DISEASES

Disease-gene associations mined from literature

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Human genes for Jackson-Weiss syndrome

Jackson-Weiss syndrome [DOID:0111337]

A syndrome characterized by craniosynostosis, midfacial hypoplasia, and foot malformations that has_material_basis_in heterozygous mutation in FGFR2 on chromosome 10q26.13.

Synonyms:  Jackson-Weiss syndrome,  DOID:0111337,  JacksonWeiss syndrome,  Jackson-Weiss disease,  Jackson-Weiss 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.