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Up to: Chromosome 7 disorder · Uniparental disomy
Paternal uniparental disomy of chromosome 7
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).
This condition has no sub-types.