paternal uniparental disomy of chromosome 5 https://www.malacards.org/card/paternal_uniparental_disomy_of_chromosome_5 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. GARD:0019339 MONDO:0019920 Orphanet:96190 icd11.foundation:1224981751 UPD(5)pat UMLS:C4749377 paternal uniparental disomy of chromosome type 5 MEDGEN:1652849 chromosome 5 disorder uniparental disomy