KEGG   DISEASE: ビオチニダーゼ欠損症
エントリ  
H01182                                                             
名称    
ビオチニダーゼ欠損症
概要    
Biotinidase deficiency is an autosomal recessive metabolic disorder in which the biotinidase is defective and the biotin is not recycled. Patients often exhibit feeding or breathing difficulties, skin rash, alopecia, hypotonia and seizures. Biotin treatment can ameliorate or prevent symptoms.
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
   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
     H01182  ビオチニダーゼ欠損症
パスウェイ 
hsa00780  Biotin metabolism
hsa04977  Vitamin digestion and absorption
病因遺伝子 
BTD [HSA:686] [KO:K01435]
コメント  
Early-onset multiple carboxylase deficiency is described in H00180. [DS:H00180]
リンク   
ICD-11: 5C50.E0
MeSH: D028921
OMIM: 253260
文献    
  著者
Wolf B
  タイトル
The neurology of biotinidase deficiency.
  雑誌
Mol Genet Metab 104:27-34 (2011)
DOI:10.1016/j.ymgme.2011.06.001
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