KEGG   DISEASE: 椎骨奇形を伴う仙骨無形成
エントリ  
H02324                                                             
名称    
椎骨奇形を伴う仙骨無形成
概要    
Sacral agenesis with vertebral anomalies is a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal. It has been reported that mutations in the T (brachyury) gene cause this disease.
カテゴリ  
先天奇形
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 20 発達異常
  多発性の発達異常または症候群
   LD2F  多発性の構造異常を伴う症候群, 主な体系の関与を伴わないもの
    H02324  椎骨奇形を伴う仙骨無形成
病因遺伝子 
TBXT [HSA:6862] [KO:K10172]
リンク   
ICD-11: LD2F.1Y
MeSH: C537221
OMIM: 615709
文献    
  著者
Postma AV, Alders M, Sylva M, Bilardo CM, Pajkrt E, van Rijn RR, Schulte-Merker S, Bulk S, Stefanovic S, Ilgun A, Barnett P, Mannens MM, Moorman AF, Oostra RJ, van Maarle MC
  タイトル
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal.
  雑誌
J Med Genet 51:90-7 (2014)
DOI:10.1136/jmedgenet-2013-102001
文献    
  著者
Giampietro PF, Raggio CL, Blank RD
  タイトル
Heterozygous mutations in the T (brachyury) gene.
  雑誌
J Med Genet 51:354 (2014)
DOI:10.1136/jmedgenet-2014-102308
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