DISEASES

Disease-gene associations mined from literature

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Human genes for ovarian hyperstimulation syndrome

Ovarian hyperstimulation syndrome [DOID:5425]

An ovarian disease that is characterized by cystic enlargement of the ovaries and a fluid shift from the intravascular to the third space and has_symptom abdominal pain, has_symptom nausea and has_symptom vomiting. This disease is an iatrogenic complication of assisted reproduction technology.

Synonyms:  ovarian hyperstimulation syndrome,  DOID:5425,  ovarian hyperstimulation disease,  ovarian hyperstimulation disorder,  ovarian hyperstimulation syndromes ...

Linkouts:  OMIM

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.