Kallmann Syndrome


Anosmic Hypogonadism

Anosmic Hypogonadisms

Anosmic Idiopathic Hypogonadotropic Hypogonadism

Autosomal Dominant Form of Kallmann Syndrome

Autosomal Recessive Form of Kallmann Syndrome

Dysplasia Olfactogenitalis of De Morsier

Hypogonadism, Anosmic

Hypogonadisms, Anosmic

Hypogonadotropic Hypogonadism and Anosmia

Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion)

Hypogonadotropic Hypogonadism-Anosmia Syndrome

Kallmann Syndrome 1

Kallmann Syndrome 2

Kallmann Syndrome 3

Kallmann Syndrome, Type 1, X-linked

Kallmann Syndrome, Type 3, Recessive

Kallmann's Syndrome

Kallmanns Syndrome

Syndrome, Kallmann

Syndrome, Kallmann's

A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait.