KEGG   DISEASE: 顔異形と小脳性運動失調を伴う脳梁無形成
エントリ  
H02396                                                             
名称    
顔異形と小脳性運動失調を伴う脳梁無形成
概要    
Corpus callosum agenesis with facial anomalies and cerebellar ataxia (CCAFCA) is a novel autosomal recessive microcephaly intellectual disability syndrome with agenesis of corpus callosum and partial hypoplasia of the vermis and cerebellum. This disease is associated with mutations in FRMD4A, that is involved in cell structure, transport and signaling.
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
   LD20  主な特徴として中枢神経系の異常を伴う症候群
    H02396  顔異形と小脳性運動失調を伴う脳梁無形成
病因遺伝子 
FRMD4A [HSA:55691] [KO:K23970]
リンク   
ICD-11: LD20.Y
OMIM: 616819
文献    
  著者
Fine D, Flusser H, Markus B, Shorer Z, Gradstein L, Khateeb S, Langer Y, Narkis G, Birk R, Galil A, Shelef I, Birk OS
  タイトル
A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A.
  雑誌
Eur J Hum Genet 23:1729-34 (2015)
DOI:10.1038/ejhg.2014.241
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