KEGG   DISEASE: 青錐体全色覚異常
エントリ  
H00974                                                             
名称    
青錐体全色覚異常
概要    
Blue cone monochromacy (also known as X-linked recessive incomplete achromatopsia) is a congenital stationary cone dysfunction syndrome characterized by the absence of both red and green cone sensitivities. Vision is derived from the remaining blue cones and rod photoreceptors. Patients present with reduced visual acuity, pendular nystagmus, and photophobia. The prevalence of blue cone monochromacy is estimated to be 1 in 100 000 males.
カテゴリ  
神経系疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 09 視覚系の疾患
  眼球後極部の疾患
   網膜の疾患
    9B70  遺伝性網膜ジストロフィ
     H00974  青錐体全色覚異常
病因遺伝子 
OPN1LW [HSA:5956] [KO:K04251]
OPN1MW [HSA:2652] [KO:K04251]
リンク   
ICD-11: 9B70
MeSH: D003117
OMIM: 303700
文献    
  著者
Simunovic MP
  タイトル
Colour vision deficiency.
  雑誌
Eye (Lond) 24:747-55 (2010)
DOI:10.1038/eye.2009.251
文献    
  著者
Gardner JC, Michaelides M, Holder GE, Kanuga N, Webb TR, Mollon JD, Moore AT, Hardcastle AJ
  タイトル
Blue cone monochromacy: causative mutations and associated phenotypes.
  雑誌
Mol Vis 15:876-84 (2009)
文献    
PMID:2788922
  著者
Nathans J, Davenport CM, Maumenee IH, Lewis RA, Hejtmancik JF, Litt M, Lovrien E, Weleber R, Bachynski B, Zwas F, et al.
  タイトル
Molecular genetics of human blue cone monochromacy.
  雑誌
Science 245:831-8 (1989)
DOI:10.1126/science.2788922
文献    
PMID:8213841 (OPN1LW OPN1MW)
  著者
Nathans J, Maumenee IH, Zrenner E, Sadowski B, Sharpe LT, Lewis RA, Hansen E, Rosenberg T, Schwartz M, Heckenlively JR, et al.
  タイトル
Genetic heterogeneity among blue-cone monochromats.
  雑誌
Am J Hum Genet 53:987-1000 (1993)
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