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Mosaic variegated aneuploidy syndrome 2

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Description

Mosaic variegated aneuploidy syndrome is an autosomal recessive disorder characterized by poor growth and variable phenotypic manifestations, such as facial dysmorphism and congenital heart defects, associated with mosaic aneuploidies resulting from defects in cell division (summary by Snape et al., 2011). See also MVA1 (257300), caused by mutation in the BUB1B gene (602860) on chromosome 15q15.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

139

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Genes

External Links

  • OMIM

    614114

  • Orphanet
  • HPO
  • Medgen

    C3279843

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