Conditions / Genetic
hypogonadotropic hypogonadism 20 with or without anosmia
info · Genetic · ICD-10: E23.0
A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGF17 gene on chromosome 8p21, sometimes in association with mutations in other genes.
Signs and symptoms
- Osteopenia
- Anosmia
- Delayed puberty
- Hypogonadism
- Osteoporosis