What is another word for Uniparental Disomy?
Pronunciation: [jˈuːnɪpˌe͡əɹəntə͡l dɪsˈɒmi] (IPA) 
Uniparental disomy refers to a rare genetic condition where an individual inherits two copies of a chromosome or a part of a chromosome from only one parent instead of one copy from each parent. This can lead to various health problems and developmental issues. Synonyms for uniparental disomy include UPD, chromosome uniparental disomy, chromosome imprinting, paternal disomy, maternal disomy, segmental uniparental disomy, and isodisomy. While these terms may differ in their specific meanings and implications, they all refer to the same basic genetic abnormality. It is important for individuals and families affected by uniparental disomy to work closely with medical professionals to understand and manage their conditions effectively.
