Acrocallosal Syndrome

MeSH 搜索器

Acrocallosal Syndrome

Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation.

推出的年份: 2009

树号: C10.500.034.500, C16.131.666.034.500

MeSH 单一 ID: D055673

进入的组:

Acrocallosal Syndromes
Syndrome, Acrocallosal
Syndromes, Acrocallosal
Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum

早前的内容:

Congenital Abnormalities (1963-2008)
Corpus Callosum (1963-2008)

All MeSH Categories
- Diseases Category
  - Nervous System Diseases [C10]
    - Nervous System Malformations [C10.500]
      - Agenesis of Corpus Callosum [C10.500.034]

All MeSH Categories
- Diseases Category
  - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
    - Congenital Abnormalities [C16.131]
      - Nervous System Malformations [C16.131.666]
        
        Agenesis of Corpus Callosum [C16.131.666.034]
        
        Acrocallosal Syndrome [C16.131.666.034.500]
        
        Aicardi Syndrome [C16.131.666.034.687]
        
        Holoprosencephaly [C16.131.666.034.875]
        
        Septo-Optic Dysplasia [C16.131.666.034.937]

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MeSH 搜索器

Acrocallosal Syndrome

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