DISEASES

Disease-gene associations mined from literature

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Human genes for Leydig cell hypoplasia

Leydig cell hypoplasia [DOID:0112259]

A pseudohermaphroditism that has_material_basis_in homozygous or compound heterozygous mutation in LHCGR on chromosome 2p16.3.

Synonyms:  Leydig cell hypoplasia,  DOID:0112259,  Leydig cell hypoplasias,  46,XY disorder of sex development due to LH resistance or LHB deficiency,  46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency ...

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.