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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
Chondrodysplasia with Joint Dislocations, Gpapp Type (CDP-GPAPP)
Alias:
Gpapp Deficiency
Chondrodysplasia with Joint Dislocations Gpapp Type
Chondrodysplasia, with Joint Dislocations, Gpapp Type
Cdp-Gpapp
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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
软骨发育不全伴关节脱位,Gpapp 型,也称为 Gpapp 缺陷,与唇裂、孤立性 Ehlers-Danlos 综合征、脊柱发育不全型 1 有关。与软骨发育不全伴关节脱位,Gpapp 型相关的基因是 BPNT2 (3'(2'),5'-磷酸核苷酶 2),其相关通路/超通路包括代谢途径生物转化 Phase I 和 II,以及胞质小分子硫酸化。相关组织包括骨,相关表型包括唇裂和小下颌。
Related ID:
MALACARDS:CHN045
OMIM:614078
MESH:D010009
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
4
20
3
CHN045
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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