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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
Arthrogryposis, Distal, Type 5 (DA5)
Alias:
Oculomelic Amyoplasia
Distal Arthrogryposis Type Iib
Distal Arthrogryposis Type 5
Arthrogryposis-Oculomotor Limitation-Electroretinal Anomalies Syndrome
Distal Arthrogryposis with Ophthalmoplegia
Distal Arthrogryposis Type 2b
Daiib
Da5
Arthrogryposis with Oculomotor Limitation and Electroretinal Abnormalities
Arthrogryposis- Oculomotor Limitation-Electroretinal Anomalies Syndrome
Arthrogryposis, Distal, Type Iib
Freeman-Sheldon Syndrome Variant
Arthrogryposis, Distal, Type 2b
Arthrogryposis, Distal, 5
Sheldon-Hall Syndrome
Da2b
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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
先天性关节挛缩,远端型5,也被称为眼球-肢体肌肉发育不良,与先天性关节挛缩,远端型2b1和先天性关节挛缩,远端型1a有关,症状包括腕部尺偏和眼肌麻痹。与先天性关节挛缩,远端型5相关的基因是PIEZO2(Piezo型机械敏感离子通道成分2),其相关通路/超级通路包括心脏传导和细胞骨架重塑,相关组织包括肺和眼,相关表型包括上睑下垂和关节僵硬。
Related ID:
MALACARDS:ART119
OMIM:108145
MESH:C537737
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
常显
新生儿
--
20
110
17
ART119
Medical Symptom
#
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
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
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Publications
No data available
References Literature
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IF
No Data Found!
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