Malformations of Cortical Development, Group II

MeSH 搜索器

Malformations of Cortical Development, Group II

Cortical malformations secondary to abnormal neuronal CELL MIGRATION in NEUROGENESIS. This group includes COBBLESTONE LISSENCEPHALY and PERIVENTRICULAR NODULAR HETEROTOPIA.

推出的年份: 2015(2008)

树号: C10.500.507.450, C16.131.666.507.450

MeSH 单一 ID: D054081

进入的组:

Malformations Secondary to Abnormal Neuronal Migration
Malformations Due to Abnormal Neuronal Migration
Cortical Malformations, Group II
Neuronal Migration Disorders
Disorder, Neuronal Migration
Disorders, Neuronal Migration
Migration Disorder, Neuronal
Migration Disorders, Neuronal
Neuronal Migration Disorder

All MeSH Categories
- Diseases Category
  - Nervous System Diseases [C10]
    - Nervous System Malformations [C10.500]
      - Malformations of Cortical Development [C10.500.507]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Congenital Abnormalities [C16.131]
      - Nervous System Malformations [C16.131.666]
        
        Malformations of Cortical Development [C16.131.666.507]
        
        Malformations of Cortical Development, Group I [C16.131.666.507.400] add_circle
        
        Malformations of Cortical Development, Group II [C16.131.666.507.450]
        
        Classical Lissencephalies and Subcortical Band Heterotopias [C16.131.666.507.450.230]
        
        Cobblestone Lissencephaly [C16.131.666.507.450.249]
        
        Lissencephaly [C16.131.666.507.450.499] add_circle
        
        Periventricular Nodular Heterotopia [C16.131.666.507.450.750]
        
        Malformations of Cortical Development, Group III [C16.131.666.507.500] add_circle

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MeSH 搜索器

Malformations of Cortical Development, Group II

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