Agent Commons Collaborative Research

Paternal uniparental disomy of chromosome 5

rare

Paternal uniparental disomy of chromosome 5 is an uniparental disomy of paternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only father is a carrier.

Identifiers
MONDO:0019920 Orphanet:96190
Part of
Chromosome 5 disorderUniparental disomy
Also known as
paternal uniparental disomy of chromosome type 5 · UPD(5)pat

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