NORD Summit 2026 Banner Ad

mosaic variegated aneuploidy syndrome 1

Download report (PDF)

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.


Resumen

Any mosaic variegated aneuploidy syndrome in which the cause of the disease is a mutation in the BUB1B gene.


Sinónimos

  • BUB1B mosaic variegated aneuploidy syndrome
  • MOSAIC variegated aneuploidy syndrome 1
  • MVA syndrome
  • MVA1
  • Mosaic variegated aneuploidy syndrome type 1
  • mosaic variegated aneuploidy syndrome 1
  • mosaic variegated aneuploidy syndrome caused by mutation in BUB1B
  • mosaic variegated aneuploidy syndrome type 1

OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

View report