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Concept information

Musculoskeletal Diseases > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Megalencephaly > Hemimegalencephaly
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Megalencephaly > Hemimegalencephaly
... > Nervous System Diseases > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group I > Megalencephaly > Hemimegalencephaly
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group I > Megalencephaly > Hemimegalencephaly

Término preferido

Hemimegalencephaly  

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Tipo

  • mesh:Descriptor

Definición

  • Rare MALFORMATIONS OF CORTICAL DEVELOPMENT, GROUP I characterized by the enlargement of one side of the brain. It is associated with seizures, partial paralysis, and mental retardation.

Concepto genérico

Etiquetas alternativas

  • Unilateral Macrocephaly
  • Unilateral Megalencephaly

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-BL458W1K-3

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RDF/XML TURTLE JSON-LD Creado 26/6/14, última modificación 1/7/19