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Brachytelephalangy characteristic facies Kallmann

Also Known As:

Brachytelephalangy with Characteristic Facies and Kallmann Syndrome; Characteristic craniofacial appearance and brachytelephalangy

Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Urogenital Diseases: 126
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
        Brachytelephalangy characteristic facies Kallmann
  - Musculoskeletal Abnormalities: 43
    - Craniofacial Abnormalities: 203
      - Brachytelephalangy characteristic facies Kallmann
- Inborn Genetic Diseases: 11939
  - Kallmann Syndrome: 376
    - Brachytelephalangy characteristic facies Kallmann
Endocrine System Diseases: 968
- Gonadal Disorders: 30
  - Hypogonadism: 6201
    - Kallmann Syndrome: 376
      - Brachytelephalangy characteristic facies Kallmann
  - Disorders of Sex Development: 730
    - 46,XY Disorder of Sex Development: 472
      - Kallmann Syndrome: 376
        Brachytelephalangy characteristic facies Kallmann
Signs and Symptoms Pathological Conditions
- Pathologic Processes: 10023
  - Disease Attributes: 18
    - Facies: 585
      - Brachytelephalangy characteristic facies Kallmann
Musculoskeletal Diseases: 719
- Musculoskeletal Abnormalities: 43
  - Craniofacial Abnormalities: 203
    - Brachytelephalangy characteristic facies Kallmann