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.

Descriptor ID	D017436
MeSH Number(s)	C12.706.316.096.750 C13.351.875.253.096.750 C16.131.939.316.096.750 C16.320.467 C19.391.119.096.750 C19.391.482.600
Concept/Terms	Kallmann Syndrome Kallmann Syndrome Syndrome, Kallmann Dysplasia Olfactogenitalis of De Morsier Kallmann's Syndrome Kallmanns Syndrome Syndrome, Kallmann's Anosmic Hypogonadism Anosmic Hypogonadisms Hypogonadism, Anosmic Hypogonadisms, Anosmic Kallmann Syndrome 2 Kallmann Syndrome 2 Autosomal Dominant Form of Kallmann Syndrome Kallmann Syndrome 3 Kallmann Syndrome 3 Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion) Kallmann Syndrome, Type 3, Recessive Autosomal Recessive Form of Kallmann Syndrome Kallmann Syndrome 1 Kallmann Syndrome 1 Kallmann Syndrome, Type 1, X-linked

Below are MeSH descriptors whose meaning is more general than "Kallmann Syndrome".

Below are MeSH descriptors whose meaning is related to "Kallmann Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Kallmann Syndrome".