DISEASES

Disease-gene associations mined from literature

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Human genes for fibular hypoplasia and complex brachydactyly

Fibular hypoplasia and complex brachydactyly [DOID:0050790]

A bone development disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly.

Synonyms:  fibular hypoplasia and complex brachydactyly,  DOID:0050790,  fibular hypoplasia and complex brachydactylies,  Du Pan syndrome,  Du Pan disease ...

Linkouts:  OMIM

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.