Microcephaly

MeSH 搜索器

Microcephaly

A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.)

推出的年份:

树号: C05.660.207.620, C10.500.507.400.500, C16.131.621.207.620, C16.131.666.507.400.500

MeSH 单一 ID: D008831

进入的组:

Microcephalies
Microlissencephaly
Microlissencephalies
Severe Congenital Microcephaly
Congenital Microcephalies, Severe
Congenital Microcephaly, Severe
Microcephalies, Severe Congenital
Microcephaly, Severe Congenital
Severe Congenital Microcephalies

All MeSH Categories
- Diseases Category
  - Musculoskeletal Diseases [C05]
    - Musculoskeletal Abnormalities [C05.660]
      - Craniofacial Abnormalities [C05.660.207]

All MeSH Categories
- Diseases Category
  - Nervous System Diseases [C10]
    - Nervous System Malformations [C10.500]
      - Malformations of Cortical Development [C10.500.507]
        
        Malformations of Cortical Development, Group I [C10.500.507.400]
        
        Megalencephaly [C10.500.507.400.249] add_circle
        
        Microcephaly [C10.500.507.400.500]
        
        Tuberous Sclerosis [C10.500.507.400.750]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Congenital Abnormalities [C16.131]
      - Musculoskeletal Abnormalities [C16.131.621]
        
        Craniofacial Abnormalities [C16.131.621.207]
        
        22q11 Deletion Syndrome [C16.131.621.207.103] add_circle
        
        Cleidocranial Dysplasia [C16.131.621.207.207]
        
        Craniofacial Dysostosis [C16.131.621.207.231] add_circle
        
        Craniosynostoses [C16.131.621.207.240] add_circle
        
        Holoprosencephaly [C16.131.621.207.410]
        
        LEOPARD Syndrome [C16.131.621.207.525]
        
        Maxillofacial Abnormalities [C16.131.621.207.540] add_circle
        
        Megalencephaly [C16.131.621.207.532] add_circle
        
        Microcephaly [C16.131.621.207.620]
        
        Porencephaly [C16.131.621.207.620.500]
        
        Noonan Syndrome [C16.131.621.207.690]
        
        Orofaciodigital Syndromes [C16.131.621.207.700]
        
        Plagiocephaly [C16.131.621.207.707] add_circle
        
        Platybasia [C16.131.621.207.720]
        
        Rubinstein-Taybi Syndrome [C16.131.621.207.850]

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]
        
        Megalencephaly [C16.131.666.507.400.249] add_circle
        
        Microcephaly [C16.131.666.507.400.500]
        
        Tuberous Sclerosis [C16.131.666.507.400.750]

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Microcephaly

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