KEGG   DISEASE: 視神経形成不全
エントリ  
H02203                                                             
名称    
視神経形成不全
  上位グループ
眼組織欠損症 [DS:H01114]
概要    
Optic nerve hypoplasia (ONH) is a congenital anomaly of the optic disc that might result in moderate to severe vision loss in children. ONH may occur as an isolated defect or in association with other ocular abnormalities, cranial abnormalities, or facial anomalies. Most of cases are sporadic, but autosomal dominant ONH have been identified. It is caused by mutations in PAX6 gene that encodes the transcription factor.
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
  主に1つの体系に影響する構造的発達異常
   眼, 眼瞼または涙器の構造的発達異常
    LA13  眼球後極部の構造的発達異常
     H02203  視神経形成不全
病因遺伝子 
PAX6 [HSA:5080] [KO:K08031]
リンク   
ICD-11: LA13.70
MeSH: C537130
OMIM: 165550
文献    
  著者
Azuma N, Yamaguchi Y, Handa H, Tadokoro K, Asaka A, Kawase E, Yamada M
  タイトル
Mutations of the PAX6 gene detected in patients with a variety of optic-nerve malformations.
  雑誌
Am J Hum Genet 72:1565-70 (2003)
DOI:10.1086/375555
文献    
  著者
Kaur S, Jain S, Sodhi HB, Rastogi A, Kamlesh
  タイトル
Optic nerve hypoplasia.
  雑誌
Oman J Ophthalmol 6:77-82 (2013)
DOI:10.4103/0974-620X.116622
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