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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Chromosome Disorders > Trisomy 18 Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Chromosome Disorders > Trisomy 18 Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Trisomy 18 Syndrome
Cardiovascular Diseases > Heart Diseases > Heart Defects, Congenital > Trisomy 18 Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Cardiovascular Abnormalities > Heart Defects, Congenital > Trisomy 18 Syndrome
Cardiovascular Diseases > Cardiovascular Abnormalities > Heart Defects, Congenital > Trisomy 18 Syndrome

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Trisomy 18 Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • A chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 18. Clinical manifestations include INTRAUTERINE GROWTH RETARDATION; CLEFT PALATE; CONGENITAL HEART DEFECTS; MICROCEPHALY; MICROGNATHIA and clenched fists with overlapping fingers. Most affected fetuses do not survive to birth. Those who survive through their first year often have severe INTELLECTUAL DISABILITY.

Concepto genérico

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URI

http://data.loterre.fr/ark:/67375/JVR-GKT5SJTB-G

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RDF/XML TURTLE JSON-LD Creado 11/7/17, última modificación 23/5/18