DISEASES

Disease-gene associations mined from literature

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Human genes for Wolf-Hirschhorn syndrome

Wolf-Hirschhorn syndrome [DOID:0050460]

A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a microdeletion of the short arm of chromosome 4.

Synonyms:  Wolf-Hirschhorn syndrome,  DOID:0050460,  WolfHirschhorn syndrome,  Wolf-Hirschhorn disease,  Wolf-Hirschhorn disorder ...

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.