DISEASES

Disease-gene associations mined from literature

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Human genes for Meckel syndrome 6

Meckel syndrome 6 [DOID:0070120]

A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32.

Synonyms:  Meckel syndrome 6,  DOID:0070120,  Meckel-Gruber syndrome, type 6,  MKS6,  MeckelGruber syndrome type 6 ...

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.