ICD-11-MMS
ICD-11-MMS ICD11分類(ICD-11-MMS) > CHAPTER20 発生異常(Developmental anomalies) > BlockL1-LD4 染色体異常、遺伝子変異を除くもの(Chromosomal anomalies, excluding gene mutations) > LD44 常染色体の欠失(Deletions of the autosomes) > LD44.H 17番染色体の欠失(Deletions of chromosome 17) > LD44.H1 17番染色体短腕の欠失(Deletions of the short arm of chromosome 17)
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LD44.H1 17番染色体短腕の欠失(Deletions of the short arm of chromosome 17)
分類ID 分類名 ICD11
1 10226130 17番染色体短腕欠失(Deletions of the short arm of chromosome 17) LD44.H1
2 20072205 17p12ーp11.2欠失(17p12-p11.2 deletion) LD44.H1
3 20072206 17p13.3端部欠失(Distal 17p13.3 deletion) LD44.H1
4 20072207 スミス・マギニス症候群(Smith-Magenis syndrome) LD44.H1
5 20072208 17p11.2欠失症候群(17p11.2 deletion syndrome) LD44.H1
6 20072209 モノソミー17p11.2(Monosomy 17p11.2) LD44.H1
7 20072210 17p11.2欠失(17p11.2 deletion) LD44.H1