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LD45.1 Uniparental disomies of paternal origin

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 the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing.

synonyms

• Uniparental disomies of paternal origin
• Paternal uniparental disomy of chromosome 1
• Paternal uniparental disomy of chromosome 4
• Paternal uniparental disomy of chromosome 5
• Paternal uniparental disomy of chromosome 6
• Paternal uniparental disomy of chromosome 7
• Paternal uniparental disomy of chromosome 11
• Paternal uniparental disomy of chromosome 13
• Paternal uniparental disomy of chromosome 14
• Paternal uniparental disomy of chromosome 15
• Paternal uniparental disomy of chromosome 20
• Paternal uniparental disomy of chromosome 21
• Paternal uniparental disomy of chromosome X

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