DISEASES

Disease-gene associations mined from literature

JensenLab
SearchDownloadsAbout

Human genes for chondrodysplasia-pseudohermaphroditism syndrome

Chondrodysplasia-pseudohermaphroditism syndrome [DOID:0060644]

A syndrome characterized by the clinical features of 46,XY complete gonadal dysgenesis in association with severe dwarfism with generalized chondrodysplasia.

Synonyms:  chondrodysplasia-pseudohermaphroditism syndrome,  DOID:0060644,  chondrodysplasiapseudohermaphroditism syndrome,  chondrodysplasia-pseudohermaphroditism disease,  chondrodysplasia-pseudohermaphroditism disorder ...

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.

Currently maintained by Qingyao Huang at Swiss Institute of Bioinformatics, University of Zurich. Licensed under CC BY 4.0.