DISEASES

Disease-gene associations mined from literature

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Human genes for nemaline myopathy 4

Nemaline myopathy 4 [DOID:0110932]

A nemaline myopathy that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13.

Synonyms:  nemaline myopathy 4,  DOID:0110932,  NEM4,  nemaline myopathy 4, autosomal dominant,  autosomal dominant nemaline myopathy 4 ...

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.