DISEASES

Disease-gene associations mined from literature

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Human genes for Meier-Gorlin syndrome 3

Meier-Gorlin syndrome 3 [DOID:0080514]

A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11.

Synonyms:  Meier-Gorlin syndrome 3,  DOID:0080514,  MeierGorlin syndrome 3

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.