KEGG   DISEASE: 膵リパーゼ欠損症
エントリ  
H02330                                                             
名称    
膵リパーゼ欠損症
概要    
Congenital pancreatic lipase deficiency is a rare autosomal recessive exocrine pancreatic failure characterized by decreased absorption of dietary fat and greasy voluminous stools, but apparent normal development and an overall good state of health. It has been reported that PNLIP mutations are causative for the phenotype.
カテゴリ  
先天性代謝異常症
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
   代謝物質の吸収または輸送の疾患
    5C62  脂質の吸収または輸送の疾患
     H02330  膵リパーゼ欠損症
パスウェイ 
hsa04977  Vitamin digestion and absorption
hsa04972  Pancreatic secretion
hsa00561  Glycerolipid metabolism
hsa04975  Fat digestion and absorption
病因遺伝子 
PNLIP [HSA:5406] [KO:K14073]
リンク   
ICD-11: 5C62
OMIM: 614338
文献    
  著者
Behar DM, Basel-Vanagaite L, Glaser F, Kaplan M, Tzur S, Magal N, Eidlitz-Markus T, Haimi-Cohen Y, Sarig G, Bormans C, Shohat M, Zeharia A
  タイトル
Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency.
  雑誌
J Lipid Res 55:307-12 (2014)
DOI:10.1194/jlr.P041103
文献    
PMID:6153713
  著者
Figarella C, De Caro A, Leupold D, Poley JR
  タイトル
Congenital pancreatic lipase deficiency.
  雑誌
J Pediatr 96:412-6 (1980)
DOI:10.1016/s0022-3476(80)80683-4
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