DISEASES

Disease-gene associations mined from literature

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Human genes for X-linked spondyloepimetaphyseal dysplasia

X-linked spondyloepimetaphyseal dysplasia [DOID:0112150]

A spondyloepimetaphyseal dysplasia that has_material_basis_in hemizygous mutation in BGN on chromosome Xq28.

Synonyms:  X-linked spondyloepimetaphyseal dysplasia,  DOID:0112150,  Xlinked spondyloepimetaphyseal dysplasia,  X-linked spondyloepimetaphyseal dysplasias,  SEMD X-linked ...

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.