DISEASES

Disease-gene associations mined from literature

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Human genes for infantile myofibromatosis

Infantile myofibromatosis [DOID:0080109]

A connective tissue benign neoplasm that is characterized by the development of benign tumors in the skin, striated muscles, bones, and in exceptional cases, visceral organs.

Synonyms:  infantile myofibromatosis,  DOID:0080109,  infantile myofibromatosises,  lipofibromatosis,  lipofibromatosises

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.