KEGG   DISEASE: メタクリル酸尿症
エントリ  
H01349                                                             
名称    
メタクリル酸尿症
概要    
Methacrylic aciduria is a very rare cerebral organic aciduria caused by 3-Hydroxy-isobutyryl-CoA hydrolase (HIBCH) mutations. HIBCH is a mitochondrial enzyme of valine catabolism. Patients demonstrated delayed development of motor skills, hypotonia, initial poor feeding, and a deterioration in neurological function during the first stages of life.
カテゴリ  
先天性代謝異常症, ミトコンドリア病
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 05 内分泌, 栄養, 代謝の疾患
  代謝疾患
   先天性代謝異常
    5C50  アミノ酸または他の有機酸代謝の先天性異常
     H01349  メタクリル酸尿症
パスウェイに基づく疾患分類 [BR:jp08402]
 アミノ酸代謝
  nt06024  バリン、ロイシン、イソロイシンの分解
   H01349  メタクリル酸尿症
パスウェイ 
hsa00280  Valine, leucine and isoleucine degradation
ネットワーク
nt06024 Valine, leucine and isoleucine degradation
病因遺伝子 
HIBCH [HSA:26275] [KO:K05605]
リンク   
ICD-11: 5C50.E
MeSH: C562803
OMIM: 250620
文献    
  著者
Loupatty FJ, Clayton PT, Ruiter JP, Ofman R, Ijlst L, Brown GK, Thorburn DR, Harris RA, Duran M, Desousa C, Krywawych S, Heales SJ, Wanders RJ
  タイトル
Mutations in the gene encoding 3-hydroxyisobutyryl-CoA hydrolase results in progressive infantile neurodegeneration.
  雑誌
Am J Hum Genet 80:195-9 (2007)
DOI:10.1086/510725
文献    
  著者
Ferdinandusse S, Waterham HR, Heales SJ, Brown GK, Hargreaves IP, Taanman JW, Gunny R, Abulhoul L, Wanders RJ, Clayton PT, Leonard JV, Rahman S
  タイトル
HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase.
  雑誌
Orphanet J Rare Dis 8:188 (2013)
DOI:10.1186/1750-1172-8-188
LinkDB    

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