DISEASES

Disease-gene associations mined from literature

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Human genes for hypogonadotropic hypogonadism 23 with or without anosmia

Hypogonadotropic hypogonadism 23 with or without anosmia [DOID:0090091]

A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13.

Synonyms:  hypogonadotropic hypogonadism 23 with or without anosmia,  DOID:0090091,  46,XY disorder of sex development due to LHB deficiency,  46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency,  46,XY DSD due to LHB 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.