KEGG   DISEASE: H00549Help
エントリ  
H00549                                                             

名称    
ファロー四徴症;
Tetralogy of Fallot
パスウェイ 
Notch シグナル伝達経路
病因遺伝子 
NKX2.5 [HSA:1482] [KO:K09345]
JAG1 [HSA:182] [KO:K06052]
ZFPM2 [HSA:23414] [KO:K17442]
GDF1 [HSA:2657] [KO:K05495]
環境要因  
Organic solvents
リンク   
ICD-10: 
OMIM: 
文献    
PMID:19818949 (gene)
  著者
Di Felice V, Zummo G
  タイトル
Tetralogy of fallot as a model to study cardiac progenitor cell migration and differentiation during heart development.
  雑誌
Trends Cardiovasc Med 19:130-5 (2009)
文献    
PMID:17924340 (gene)
  著者
Karkera JD, Lee JS, Roessler E, Banerjee-Basu S, Ouspenskaia MV, Mez J, Goldmuntz E, Bowers P, Towbin J, Belmont JW, Baxevanis AD, Schier AF, Muenke M
  タイトル
Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans.
  雑誌
Am J Hum Genet 81:987-94 (2007)
文献    
PMID:17519397 (env_factor)
  著者
Jenkins KJ, Correa A, Feinstein JA, Botto L, Britt AE, Daniels SR, Elixson M, Warnes CA, Webb CL
  タイトル
Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on  Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
  雑誌
Circulation 115:2995-3014 (2007)

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