Structured Summary
Abstract
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.
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Synonyms
20 entry terms
- Anosmic Hypogonadism
- Anosmic Idiopathic Hypogonadotropic Hypogonadism
- Dysplasia Olfactogenitalis of De Morsier
- Hypogonadotropic Hypogonadism and Anosmia
- Hypogonadotropic Hypogonadism-Anosmia Syndrome
- Kallmann's Syndrome
- Anosmic Hypogonadisms
- Hypogonadism, Anosmic
- Hypogonadisms, Anosmic
- Kallmanns Syndrome
- Syndrome, Kallmann
- Syndrome, Kallmann's
- Autosomal Dominant Form of Kallmann Syndrome
- Autosomal Recessive Form of Kallmann Syndrome
- Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion)
- Kallmann Syndrome 1
- Kallmann Syndrome 2
- Kallmann Syndrome 3
- Kallmann Syndrome, Type 1, X-linked
- Kallmann Syndrome, Type 3, Recessive
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
93
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Previous Indexing
- Hypogonadism (1966-1992)
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References
- National Library of Medicine. Kallmann Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D017436. http://id.nlm.nih.gov/mesh/2026/D017436
- Kallmann Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Kallmann_syndrome
- Kallmann Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q1165179