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).
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paternal uniparental disomy of chromosome 14
MONDO:0011975
ring chromosome 7
MONDO:0015441
mosaic trisomy 7
MONDO:0015771
silver-Russell syndrome due to maternal uniparental disomy of chromosome 11
MONDO:0016482
paternal uniparental disomy of chromosome 1
MONDO:0016650
maternal uniparental disomy of chromosome 1
MONDO:0016651