trisomy 22
partial or complete triplication of chromosome 22
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trisomy 22
Summary
trisomy 22 is a rare disease[1]. It draws 82 Wikipedia views per month (rare_disease category, ranking #183 of 627).[2]
Key Facts
- trisomy 22's instance of is recorded as rare disease[3].
- trisomy 22's instance of is recorded as developmental defect during embryogenesis[4].
- trisomy 22's subclass of is recorded as autosomal trisomy[5].
- trisomy 22's DiseasesDB is recorded as 32684[6].
- trisomy 22's Freebase ID is recorded as /m/02w9wv7[7].
- trisomy 22's chromosome is recorded as human chromosome 22[8].
- trisomy 22's NCI Thesaurus ID is recorded as C114765[9].
- trisomy 22's health specialty is recorded as medical genetics[10].
- trisomy 22's UMLS CUI is recorded as C0265490[11].
- trisomy 22's GARD rare disease ID is recorded as 5335[12].
- trisomy 22's Mondo ID is recorded as MONDO_0022759[13].
- trisomy 22's Microsoft Academic ID is recorded as 2777222132[14].
Why It Matters
trisomy 22 draws 82 Wikipedia views per month (rare_disease category, ranking #183 of 627).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[15]