paternal uniparental disomy of chromosome 7
MONDO:0019922Mondo
Findings
No curated finding names paternal uniparental disomy of chromosome 7 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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).
Definition from the Mondo Disease Ontology (MONDO:0019922), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
2 names
Resolves to: paternal uniparental disomy of chromosome 7
- Also called
- paternal uniparental disomy of chromosome type 7UPD(7)pat