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Isolated follicle stimulating hormone deficiency
1 OMIM reference -
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
46,XX gonadal dysgenesis
Ovarian hyperstimulation syndrome
Synonym(s):
- Isolated FSH deficiency
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare infertility
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: C537070
Gene symbol UniProt reference OMIM reference
FSHB P01225136530
No signs/symptoms info available.