KEGG   DISEASE: 肢端骨異形成
エントリ  
H02229                                                             
名称    
肢端骨異形成;
肢端骨異形成および色素異常
概要    
Terminal osseous dysplasia (TOD) is an X-linked dominant male-lethal disease characterized by skeletal dysplasia of the limbs, pigmentary defects of the skin, and recurrent digital fibroma with onset in female infancy. TOD is caused by a mutation in the FLNA gene.
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
   LD24  主な特徴として骨格の異常を伴う症候群
    H02229  肢端骨異形成
病因遺伝子 
FLNA [HSA:2316] [KO:K04437]
リンク   
ICD-11: LD24.8Y
MeSH: C564554
OMIM: 300244
文献    
  著者
Baroncini A, Castelluccio P, Morleo M, Soli F, Franco B
  タイトル
Terminal osseous dysplasia with pigmentary defects: clinical description of a new family.
  雑誌
Am J Med Genet A 143A:51-7 (2007)
DOI:10.1002/ajmg.a.31557
文献    
  著者
Sun Y, Almomani R, Aten E, Celli J, van der Heijden J, Venselaar H, Robertson SP, Baroncini A, Franco B, Basel-Vanagaite L, Horii E, Drut R, Ariyurek Y, den Dunnen JT, Breuning MH
  タイトル
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA gene.
  雑誌
Am J Hum Genet 87:146-53 (2010)
DOI:10.1016/j.ajhg.2010.06.008
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