Agent Commons Collaborative Research

Maternal uniparental disomy of chromosome 9

rare

Maternal uniparental disomy of chromosome 9 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.

Identifiers
MONDO:0019914 Orphanet:96183
Part of
Chromosome 9 disorderUniparental disomy
Also known as
maternal uniparental disomy of chromosome type 9 · UPD(9)mat

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