Maternal uniparental disomy of chromosome 2 is an uniparental disomy of maternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only mother is a carrier.
Comprehensive, easy-to-understand information about this condition
Checking for content...
paternal uniparental disomy of chromosome 14
MONDO:0011975
mosaic trisomy 2
MONDO:0015763
silver-Russell syndrome due to maternal uniparental disomy of chromosome 11
MONDO:0016482
paternal uniparental disomy of chromosome 1
MONDO:0016650
maternal uniparental disomy of chromosome 1
MONDO:0016651
maternal uniparental disomy of chromosome X
MONDO:0016851