DISEASES

Disease-gene associations mined from literature

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Human genes for Kallmann syndrome

Kallmann syndrome [DOID:3614]

A hypogonadotropic hypogonadism with a defective sense of smell (anosmia or hyposmia).

Synonyms:  Kallmann syndrome,  DOID:3614,  Kallmann disease,  Kallmann disorder,  Kallmann syndromes ...

Linkouts:  OMIM #1 #2 #3 #4 #5

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.