Klippel-Feil Syndrome

MeSH 搜索器

Klippel-Feil Syndrome

A syndrome characterised by a low hairline and a shortened neck resulting from a reduced number of vertebrae or the fusion of multiple hemivertebrae into one osseous mass.

推出的年份:

树号: C05.116.099.370.535, C05.660.551, C16.131.621.551

MeSH 单一 ID: D007714

进入的组:

Klippel Feil Syndrome
Syndrome, Klippel-Feil
Vertebral Cervical Fusion Syndrome
Klippel-Feil Sequence
Dystrophia Brevicollis Congenita
Dystrophia Brevicollis Congenitas
Cervical Fusion Syndrome

All MeSH Categories
- Diseases Category
  - Musculoskeletal Diseases [C05]
    - Bone Diseases [C05.116]
      - Bone Diseases, Developmental [C05.116.099]
        
        Dysostoses [C05.116.099.370]
        
        Craniofacial Dysostosis [C05.116.099.370.231] add_circle
        
        Focal Dermal Hypoplasia [C05.116.099.370.380]
        
        Klippel-Feil Syndrome [C05.116.099.370.535]
        
        Orofaciodigital Syndromes [C05.116.099.370.652]
        
        Rubinstein-Taybi Syndrome [C05.116.099.370.797]
        
        Synostosis [C05.116.099.370.894] add_circle

All MeSH Categories
- Diseases Category
  - Musculoskeletal Diseases [C05]
    - Musculoskeletal Abnormalities [C05.660]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Congenital Abnormalities [C16.131]
      - Musculoskeletal Abnormalities [C16.131.621]

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MeSH 搜索器

Klippel-Feil Syndrome

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