LD45.0 Uniparental disomies of maternal origin
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Any disease characterised by the inheritance of two homologous copies of a chromosome from the mother, and none from the father. Confirmation is by observation of identical chromosome pairs, and matching to a maternal chromosome, by genetic testing.
synonyms
- Uniparental disomies of maternal origin
- Maternal uniparental disomy of chromosome 1
- Maternal uniparental disomy of chromosome 2
- Maternal uniparental disomy of chromosome 4
- Maternal uniparental disomy of chromosome 6
- Maternal uniparental disomy of chromosome 7
- Maternal uniparental disomy of chromosome 9
- Maternal uniparental disomy of chromosome 11
- Maternal uniparental disomy of chromosome 13
- Maternal uniparental disomy of chromosome 14
- Maternal uniparental disomy of chromosome 15
- Maternal uniparental disomy of chromosome 16
- Maternal uniparental disomy of chromosome 20
- Maternal uniparental disomy of chromosome 21
- Maternal uniparental disomy of chromosome 22
- Maternal uniparental disomy of chromosome X
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