KEGG   DISEASE: 網膜色素変性症を伴う後索型失調症
エントリ  
H01036                                                             
名称    
網膜色素変性症を伴う後索型失調症
概要    
Posterior column ataxia with retinitis pigmentosa (PCARP) is an autosomal recessive, childhood onset neurodegenerative disorder characterized by sensory ataxia and retinitis pigmentosa. It has been reported that PCARP is caused by mutations in FLVCR1, a gene encoding a heme-transporter protein.
カテゴリ  
神経系疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 08 神経系の疾患
  運動障害
   8A03  失調性障害
    H01036  網膜色素変性症を伴う後索型失調症
病因遺伝子 
FLVCR1 [HSA:28982] [KO:K08220]
リンク   
ICD-11: 8A03.1Y
MeSH: C536343
OMIM: 609033
文献    
  著者
Ishiura H, Fukuda Y, Mitsui J, Nakahara Y, Ahsan B, Takahashi Y, Ichikawa Y, Goto J, Sakai T, Tsuji S
  タイトル
Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1.
  雑誌
Neurogenetics 12:117-21 (2011)
DOI:10.1007/s10048-010-0271-4
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