DISEASES

Disease-gene associations mined from literature

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Human genes for Greig cephalopolysyndactyly syndrome

Greig cephalopolysyndactyly syndrome [DOID:14761]

An acrocephalosyndactylia that has_material_basis_in mutation in the GLI3 gene which results_in abnormal development located_in limb, located_in head, located_in face.

Synonyms:  Greig cephalopolysyndactyly syndrome,  DOID:14761,  Greig cephalopolysyndactyly disease,  Greig cephalopolysyndactyly disorder,  Greig cephalopolysyndactyly syndromes ...

Linkouts:  OMIM

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.