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Concept information

disease > complex syndrome > contiguous gene syndrome
... > disease > genetic disease > chromosomal aberration > abnormal chromosome > deletion > contiguous gene syndrome

Terme préférentiel

contiguous gene syndrome  

Définition

  • A contiguous gene syndrome (CGS), also known as a contiguous gene deletion syndrome is a clinical phenotype caused by a chromosomal abnormality, such as a deletion or duplication that removes several genes lying in close proximity to one another on the chromosome. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-ZLR2Q92T-B

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