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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
Macular Dystrophy, Corneal (MCD)
Alias:
Macular Corneal Dystrophy
Mcd
Fehr Corneal Dystrophy
Groenouw Type Ii Corneal Dystrophy
Corneal Dystrophy Groenouw Type Ii
Macular Corneal Dystrophy, Type Ii
Macular Corneal Dystrophy Type Ii
Corneal Dystrophy, Macular Type
Macular Corneal Dystrophy, Type I
Macular Dystrophy, Corneal Type 1
Macular Corneal Dystrophy Type I
Corneal Dystrophy Macular Type
Macular Dystrophy, Corneal, 1
Dystrophy, Macular, Corneal
Mcdc1, Formerly
Mcdc1
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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
黄斑部角膜病变,又称黄斑角膜病变,与角膜病变、梅斯曼1型和埃勒斯-当洛斯综合症、脊柱发育不良型1型有关。与黄斑部角膜病变相关的基因有CHST6(糖基硫酸转移酶6),其相关通路/超通路包括代谢和代谢途径生物转化I和II期。在该疾病的背景下提到了Fomepizole和保护剂。相关组织包括眼睛和内皮,相关表型为角膜基质的混浊和角膜结晶。
Related ID:
MALACARDS:MCL075
OMIM:217800
MESH:D003317
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
全年龄段
--
15
76
43
MCL075
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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