Uniparental disomies
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Any disease caused by the inheritance of two homologous copies of a chromosome from one parent, and none from the other parent. Confirmation is by observation of identical chromosomes pairs by genetic testing.
sections/codes in this section (LD45-LD45)
- Uniparental disomies of maternal origin (LD45.0)
- Uniparental disomies of paternal origin (LD45.1)
- Other specified uniparental disomies (LD45.Y)
- Uniparental disomies, unspecified (LD45.Z)
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