DISEASES

Disease-gene associations mined from literature

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Human genes for Norman-Roberts syndrome

Norman-Roberts syndrome [DOID:0060902]

A lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22.

Synonyms:  Norman-Roberts syndrome,  DOID:0060902,  NormanRoberts syndrome,  Norman-Roberts disease,  Norman-Roberts disorder ...

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.