uniparental disomy
presence in a cell of two paired chromosomes from the same parent, with no chromosome of that pair from the other parent
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uniparental disomy
Summary
uniparental disomy ranks in the top 2% of general entities by monthly Wikipedia readership (58 views/month).[1]
Key Facts
- uniparental disomy's subclass of is recorded as chromosome abnormality[2].
- uniparental disomy's MeSH descriptor ID is recorded as D024182[3].
- uniparental disomy's ICD-10 ID is recorded as Q99.8[4].
- uniparental disomy's Freebase ID is recorded as /m/01_0g4[5].
- uniparental disomy's MeSH tree code is recorded as C23.550.210.645.890[6].
- uniparental disomy's MeSH tree code is recorded as G05.365.590.175.935[7].
- uniparental disomy's Gran Enciclopèdia Catalana ID is recorded as 0271245[8].
- uniparental disomy's Encyclopædia Britannica Online ID is recorded as topic/uniparental-disomy[9].
- uniparental disomy's Microsoft Academic ID is recorded as 2780332060[10].
- uniparental disomy's ICD-11 ID is recorded as LD45[11].
- uniparental disomy's ICD-11 ID is recorded as 694223526[12].
- uniparental disomy's OpenAlex ID is recorded as C2780332060[13].
- uniparental disomy's Gran Enciclopèdia Catalana ID is recorded as disomia-uniparental[14].
Why It Matters
uniparental disomy ranks in the top 2% of general entities by monthly Wikipedia readership (58 views/month).[1] It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[15] It is known by 12 alternative names across languages and contexts.[16]