DISEASES

Disease-gene associations mined from literature

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Human genes for Noonan syndrome with multiple lentigines 2

Noonan syndrome with multiple lentigines 2 [DOID:0080549]

A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the RAF1 gene on chromosome 3p25.

Synonyms:  Noonan syndrome with multiple lentigines 2,  DOID:0080549,  LEOPARD syndrome 2

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.