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

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.