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Hypogonadismus, hypogonadotroper normosmischer, kongenitale Form

ORPHA:432· ICD-10 E23.0· Normosmic congenital hypogonadotropic hypogonadism

Vererbung
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive
Erkrankungsalter
Infancy, Neonatal