trisomy 16

Summary

trisomy 16 is a rare disease^[1]. It draws 182 Wikipedia views per month (rare_disease category, ranking #141 of 627).^[2]

Key Facts

• trisomy 16's instance of is recorded as rare disease^[3].
• trisomy 16's instance of is recorded as developmental defect during embryogenesis^[4].
• trisomy 16's instance of is recorded as class of disease^[5].
• trisomy 16's subclass of is recorded as total autosomal trisomy^[6].
• trisomy 16's MeSH descriptor ID is recorded as C538041^[7].
• trisomy 16's chromosome is recorded as human chromosome 16^[8].
• trisomy 16's Orphanet ID is recorded as 1708^[9].
• trisomy 16's NCI Thesaurus ID is recorded as C37866^[10].
• trisomy 16's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1708^[11].
• trisomy 16's UMLS CUI is recorded as C1519651^[12].
• trisomy 16's UMLS CUI is recorded as C4707009^[13].
• trisomy 16's ICD-10-CM is recorded as Q92.1^[14].
• trisomy 16's GARD rare disease ID is recorded as 7060^[15].
• trisomy 16's Mondo ID is recorded as MONDO_0015729^[16].
• trisomy 16's Microsoft Academic ID is recorded as 2779658141^[17].

Why It Matters

trisomy 16 draws 182 Wikipedia views per month (rare_disease category, ranking #141 of 627).^[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.^[18] It is known by 5 alternative names across languages and contexts.^[19]