KEGG   DISEASE: 網膜ジストロフィー、若年性白内障、低身長症候群
エントリ  
H02292                                                             
名称    
網膜ジストロフィー、若年性白内障、低身長症候群
概要    
Retinal dystrophy, juvenile cataracts, and short stature syndrome (RDJCSS) is an autosomal recessive retinitis pigmentosa with systemic features, including facial dysmorphologies, psychomotor developmental delays, learning disabilities and short stature. RDJCSS is caused by nonsense mutations in retinol dehydrogenase RDH11. In the eye, RDH11 has an oxidoreductive function in the visual cycle.
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
   LD21  主な特徴として眼の異常を伴う症候群
    H02292  網膜ジストロフィー、若年性白内障、低身長症候群
パスウェイ 
hsa00830  Retinol metabolism
病因遺伝子 
RDH11 [HSA:51109] [KO:K11152]
リンク   
ICD-11: LD21.Y
OMIM: 616108
文献    
  著者
Xie YA, Lee W, Cai C, Gambin T, Noupuu K, Sujirakul T, Ayuso C, Jhangiani S, Muzny D, Boerwinkle E, Gibbs R, Greenstein VC, Lupski JR, Tsang SH, Allikmets R
  タイトル
New syndrome with retinitis pigmentosa is caused by nonsense mutations in retinol dehydrogenase RDH11.
  雑誌
Hum Mol Genet 23:5774-80 (2014)
DOI:10.1093/hmg/ddu291
LinkDB    

» English version

DBGET integrated database retrieval system