Kallmann syndrome

Orpha code: 478OMIM code: 615271

Definition

Kallmann syndrome (KS) is a developmental genetic disorder characterized by the association of congenital hypogonadotropic hypogonadism (CHH) due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs).

Disease data
Classification

Clinical subtype

Synonyms
Congenital hypogonadotropic hypogonadism with anosmia
Patologiczna sekwencja węchowo-płciowa
Wrodzony hipogonadyzm hipogonadotropowy z anosmią
Olfacto-genital pathological sequence
ORPHA code
478
OMIM code
615271
ICD10 code
E23.0
ICD11 code
5A61.2

No additional description.

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