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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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