DISEASES

Disease-gene associations mined from literature

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Human genes for spondyloepiphyseal dysplasia tarda

Spondyloepiphyseal dysplasia tarda [DOID:0112284]

A spondyloepiphyseal dysplasia characterized by impaired growth of the bones of the spine and the ends of the long bones that becomes apparent in after birth.

Synonyms:  spondyloepiphyseal dysplasia tarda,  DOID:0112284,  spondyloepiphyseal dysplasia tardas

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.