Cytoscape Web
Click node...

Ovarian hyperstimulation syndrome
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
46,XX gonadal dysgenesis
Isolated follicle stimulating hormone deficiency
Familial partial lipodystrophy due to AKT2 mutations
Hypoinsulinemic hypoglycemia and body hemihypertrophy
Acute promyelocytic leukemia
Alveolar rhabdomyosarcoma
Synonym(s):
- OHSS
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D016471
Gene symbol UniProt reference OMIM reference
FSHR P23945136435
No signs/symptoms info available.