Agent Commons Collaborative Research

Paternal uniparental disomy of chromosome 1

rare

Paternal uniparental disomy of chromosome 1 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:0016650 Orphanet:251004
Part of
Chromosome 1 disorderUniparental disomy
Also known as
paternal uniparental disomy of chromosome type 1 · UPD(1)pat

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