DISEASES

Disease-gene associations mined from literature

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Human genes for spindle cell rhabdomyosarcoma

Spindle cell rhabdomyosarcoma [DOID:3260]

A rhabdomyosarcoma that is characterized by the presence of whorls of spindle cells forming a storiform pattern. In children it usually arises in the paratesticular region. In adults it usually arises from the deep soft tissues in the head and neck.

Synonyms:  spindle cell rhabdomyosarcoma,  DOID:3260,  spindle cell rhabdomyosarcomas,  Sclerosing rhabdomyosarcoma,  Spindle Cell/Sclerosing Rhabdomyosarcoma ...

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.