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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
Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a (CPSFS1A)
Alias:
Multiple Pterygium Syndrome, Autosomal Dominant
Contractures, Pterygia, and Spondylocarpostarsal Fusion Syndrome 1a
Autosomal Dominant Multiple Pterygium Syndrome
Cpsfs1a
Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a
Pterygium Syndrome, Multiple, Autosomal Dominant
Arthrogryposis, Distal, Type 8, Formerly
Arthrogryposis, Distal, Type 8
Pterygium Syndrome, Multiple
Distal Arthrogryposis Type 8
Autosomal Dominant
Da8, Formerly
Cpskf1a
Da8
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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
挛缩、翼状胬肉和脊柱-掌骨-跖骨融合综合征1a,也称为多翼状胬肉综合征,常染色体显性遗传,与常染色体显性多囊肾病和低钙血症1有关。与挛缩、翼状胬肉和脊柱-掌骨-跖骨融合综合征1a有关的重要基因是MYH3(肌球蛋白重链3)。在该疾病的背景下,已提到的药物包括血管紧张素II和坎地沙坦酯。附属组织包括肾脏和肝脏,相关表型为短颈和听力障碍。
Related ID:
MALACARDS:CNT116
OMIM:178110
MESH:D001176
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
孩童期
<1/1000000
1
4
10
CNT116
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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