haploinsufficiency
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haploinsufficiency
Summary
haploinsufficiency ranks in the top 2% of general entities by monthly Wikipedia readership (87 views/month).[1]
Key Facts
- haploinsufficiency's subclass of is recorded as loss of heterozygosity[2].
- haploinsufficiency's Commons category is recorded as Haploinsufficiency[3].
- haploinsufficiency's MeSH descriptor ID is recorded as D057895[4].
- haploinsufficiency's Freebase ID is recorded as /m/066vzg[5].
- haploinsufficiency's MeSH tree code is recorded as G05.365.590.029.530.587[6].
- haploinsufficiency's MeSH tree code is recorded as G05.380.350.500[7].
- haploinsufficiency's facet of is recorded as gene dosage[8].
- haploinsufficiency's NALT ID is recorded as 324466[9].
- haploinsufficiency's UMLS CUI is recorded as C2936267[10].
- haploinsufficiency's JSTOR topic ID is recorded as haploinsufficiency[11].
- haploinsufficiency's Microsoft Academic ID is recorded as 68838962[12].
- haploinsufficiency's DeCS ID is recorded as 54332[13].
- haploinsufficiency's OpenAlex ID is recorded as C68838962[14].
- haploinsufficiency's NCI Dictionary of Genetics Terms entry is recorded as haploinsufficiency[15].
Why It Matters
haploinsufficiency ranks in the top 2% of general entities by monthly Wikipedia readership (87 views/month).[1] haploinsufficiency has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[16] haploinsufficiency is known by 3 alternative names across languages and contexts.[17]