Complete trisomy 18 (Q46806)

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Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterised by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations.
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LD40.2
    English
    Complete trisomy 18
    Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterised by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations.

      Statements

      CID11:LD40.2
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      dki-india-LD40.2
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      Concluído
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      13 August 2026
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