pentasomy X
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pentasomy X
Summary
pentasomy X is a rare disease[1]. It draws 589 Wikipedia views per month (rare_disease category, ranking #128 of 627).[2]
Key Facts
- pentasomy X's instance of is recorded as rare disease[3].
- pentasomy X's instance of is recorded as chromosomal disease[4].
- pentasomy X's instance of is recorded as developmental defect during embryogenesis[5].
- pentasomy X's instance of is recorded as class of disease[6].
- pentasomy X is a type of sex chromosome disorder[7].
- pentasomy X is a type of polysomy of X chromosome[8].
- pentasomy X's Commons category is recorded as Pentasomy X[9].
- pentasomy X's ICPC 2 ID is recorded as A90[10].
- pentasomy X's facet of is recorded as women's health[11].
- pentasomy X's NCI Thesaurus ID is recorded as C89802[12].
- pentasomy X's health specialty is recorded as medical genetics[13].
- pentasomy X's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_11[14].
- pentasomy X's on focus list of Wikimedia project is recorded as gender gap on Dutch Wikipedia[15].
Why It Matters
pentasomy X draws 589 Wikipedia views per month (rare_disease category, ranking #128 of 627).[2] It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[16] It is known by 28 alternative names across languages and contexts.[17]