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]

An acromesomelic dysplasia that is characterized 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,  acromesomelic dysplasia-2B ...

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.

Currently maintained by Qingyao Huang at Swiss Institute of Bioinformatics, University of Zurich. Licensed under CC BY 4.0.