Sveinsson Chorioretinal Atrophy (SCRA)

Sveinsson Chorioretinal Atrophy(来自ICD-11)
别称:
Helicoid Peripapillary Chorioretinal Degeneration
Atrophia Areata
Scra
Hpcd
Peripapillary Chorioretinal Degeneration, Icelandic Type
Helicoidal Peripapillary Chorioretinal Degeneration
Aa
Atrophy, Chorioretinal, Sveinsson
加入收藏
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Sveinsson Chorioretinal Atrophy, also known as helicoid peripapillary chorioretinal degeneration, is related to choroidal dystrophy, central areolar, 1 and abetalipoproteinemia. An important gene associated with Sveinsson Chorioretinal Atrophy is TEAD1 (TEA Domain Transcription Factor 1), and among its related pathways/superpathways are Signal Transduction and Pleural mesothelioma. Affiliated tissues include eye and retina, and related phenotypes are myopia and astigmatism
查看原文 参与反馈
相关ID:

基础信息

遗传方式
发病时间
患病率/发病率
相关基因
相关模型
参考文献
MALACARDS
AD
Unknown
<1/1000000
23
197
9

疾病表征

#
分类
表征
HPO概率
Orphanet概率
HPO来源
暂无相关数据

基因 & 突变

#
基因
作用分类
分值
突变数量
暂无相关数据

靶点药物

药物名称
CAS号
研发状态
临床阶段
暂无相关数据

疾病模型

类型
名称
MGI
相关基因
品系来源
文献数量
暂无相关数据

文献报道

标题
PMID
期刊
年代
IF
暂无数据
Wechat
Comparison
Al agent
Tutorials
Back to top