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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Achromatopsia (ACHM)
Alias:
Total Color Blindness
Rod Monochromatism
Rod Monochromacy
Achm
Complete or Incomplete Color Blindness
Pingelapese Blindness
Achromatopsia 2
Achromatopsia 3
Achromatopsia 1
Monochromatism
Achromatism
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
无色性视觉障碍,也被称为全色盲,与无色性视觉障碍2和无色性视觉障碍3有关,症状包括畏光。与无色性视觉障碍相关的基因是PDE6C(磷酸二酯酶6C),其相关通路/超级通路包括嗅觉信号通路和CREB通路。在该疾病的背景下提到了苯基丁酸和甘油。附属组织包括眼睛和视网膜,相关表型包括畏光和色觉缺陷。
Related ID:
MALACARDS:ACH003
MESH:D003117
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
1-9/100000
70
561
91
ACH003
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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