Paternal uniparental disomy of chromosome 7 is an uniparental disomy of paternal origin that most likely do not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only father is a carrier (e.g., cystic fibrosis, congenital chloride diarrhea, sensorineural hearing loss). The disease is Monarch Disease Ontology identifier MONDO_0019922 (paternal uniparental disomy of chromosome 7). Also known as: UPD(7)pat, paternal uniparental disomy of chromosome type 7.