Kallmann Syndrome

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.

Also Known As:

Kallmann's Syndrome; Anosmic Hypogonadism; Anosmic Idiopathic Hypogonadotropic Hypogonadism; Autosomal Dominant Form of Kallmann Syndrome; Autosomal Recessive Form of Kallmann Syndrome; Dysplasia Olfactogenitalis of De Morsier; 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; Anosmic Hypogonadisms; Hypogonadism, Anosmic; Hypogonadisms, Anosmic; Kallmanns Syndrome; Syndrome, Kallmann; Syndrome, Kallmann's

Urogenital Diseases: 126
- Urogenital Abnormalities: 76
  - Disorders of Sex Development: 730
    - 46,XY Disorder of Sex Development: 472
      - Kallmann Syndrome: 376
- Female Urogenital Diseases and Pregnancy Complications
  - Female Urogenital Diseases
    - Urogenital Abnormalities: 76
      - Disorders of Sex Development: 730
        46,XY Disorder of Sex Development: 472
        Kallmann Syndrome: 376
- Male Urogenital Diseases
  - Urogenital Abnormalities: 76
    - Disorders of Sex Development: 730
      - 46,XY Disorder of Sex Development: 472
        Kallmann Syndrome: 376
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Urogenital Abnormalities: 76
    - Disorders of Sex Development: 730
      - 46,XY Disorder of Sex Development: 472
        Kallmann Syndrome: 376
- Inborn Genetic Diseases: 11939
  - Kallmann Syndrome: 376
Endocrine System Diseases: 968
- Gonadal Disorders: 30
  - Hypogonadism: 6201
    - Kallmann Syndrome: 376
  - Disorders of Sex Development: 730
    - 46,XY Disorder of Sex Development: 472
      - Kallmann Syndrome: 376

Carine Monnier Selected Research

Carine Monnier Research Topics

Disease

Drug/Important Bio-Agent (IBA)