Bestrophinopathy，常染色体隐性遗传
基因病名称(英)
Bestrophinopathy, autosomal recessive
基因病名称
Bestrophinopathy，常染色体隐性遗传
别名(英)
Bestrophinopathy,Retinopathy Burgess-Black type
别名
Bestrophinopathy,Retinopathy Burgess-Black 型
统计
reviewed:1; annotated:0
交叉引用
611809,C2678493,D012164
描述(英)
A retinopathy characterized by loss of central vision, an absent electro-oculogram light rise, and electroretinogram anomalies.
描述
一种以中心视力丧失、眼电图光上升缺失和视网膜电图异常为特征的视网膜病变。