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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
Coloboma, Ocular, Autosomal Dominant (COAD)
Alias:
Coloboma, Ocular
Coloboma of Iris, Choroid, and Retina
Coi
Chronic Obstructive Airway Disease
Coloboma of Choroid and Retina
Congenital Ocular Coloboma
Chorioretinal Coloboma
Coloboma, Uveoretinal
Uveoretinal Coloboma
Ocular Coloboma
Coad
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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
先天性虹膜缺损,常染色体显性遗传,也称为先天性虹膜缺损,与Macs综合症和眼晶状体缺损有关,症状包括心绞痛、咳嗽和打鼾。与先天性虹膜缺损相关的基因是PAX6(配对盒6),其相关通路/超级通路包括神经系统发育和Wnt / Hedgehog / Notch。在该疾病的背景下提到了药物Tiotropium和一氧化氮。相关组织包括视网膜和眼睛,相关表型为眼球震颤和角膜混浊。
Related ID:
MALACARDS:CLB034
OMIM:120200
MESH:D003103
ICD11:20223105
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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17
181
16
CLB034
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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