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:
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

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
No Data Found!
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