trisomy 16
partial or complete triplication of chromosome 16
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trisomy 16
Summary
trisomy 16 is a rare disease[1]. It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[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 is a type of total autosomal trisomy[6].
- trisomy 16's chromosome is recorded as human chromosome 16[7].
- trisomy 16's NCI Thesaurus ID is recorded as C37866[8].
- trisomy 16's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1708[9].
Why It Matters
trisomy 16 has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2] It is known by 5 alternative names across languages and contexts.[10]