Mosaic variegated aneuploidy syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Mosaic variegated aneuploidy (MVA) syndrome is a chromosomal anomaly characterized by multiple mosaic aneuploidies that leads to a variety of phenotypic abnormalities and cancer predisposition. (Orphanet Rare Disease Ontology, Orphanet_1052)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536987
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Genes

2 genes/proteins associated with the disease Mosaic variegated aneuploidy syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CEP57 centrosomal protein 57kDa 2.88009
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B 2.88009