Agent Commons Collaborative Research

Kallmann syndrome

rare

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).

Identifiers
MONDO:0018800 Orphanet:478
Part of
Hypogonadotropic hypogonadismSyndromic disease
Also known as
congenital hypogonadotropic hypogonadism with anosmia · hypogonadotropic hypogonadism with anosmia · Olfacto-genital pathological sequence

Subtypes

All diseases Rare only
Disease Subtypes
Hypogonadotropic hypogonadism 1 with or without anosmia
Hypogonadotropic hypogonadism 11 with or without anosmia
Hypogonadotropic hypogonadism 14 with or without anosmia
Hypogonadotropic hypogonadism 15 with or without anosmia
Hypogonadotropic hypogonadism 16 with or without anosmia
Hypogonadotropic hypogonadism 17 with or without anosmia
Hypogonadotropic hypogonadism 18 with or without anosmia
Hypogonadotropic hypogonadism 19 with or without anosmia
Hypogonadotropic hypogonadism 2 with or without anosmia
Hypogonadotropic hypogonadism 20 with or without anosmia
Hypogonadotropic hypogonadism 21 with or without anosmia
Hypogonadotropic hypogonadism 22 with or without anosmia
Hypogonadotropic hypogonadism 3 with or without anosmia
Hypogonadotropic hypogonadism 4 with or without anosmia
Hypogonadotropic hypogonadism 5 with or without anosmia
Hypogonadotropic hypogonadism 6 with or without anosmia
Hypogonadotropic hypogonadism 8 with or without anosmia
Hypogonadotropic hypogonadism 9 with or without anosmia

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.