Prolidase Deficiency (PD)

Alias:
Hyperimidodipeptiduria
Imidodipeptidase Deficiency
Peptidase Deficiency
Pd
Proline Dipeptidase Deficiency
Deficiency of Prolidase
Imidodipeptiduria
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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
脯氨酰二肽酶缺乏症,又称高咪唑二肽尿症,与阵发性极端疼痛障碍和脾肿大有关,症状包括皮肤紫癜。与脯氨酰二肽酶缺乏症相关的重要基因是PEPD(肽酶D),其相关通路/超级通路包括22q11.2拷贝数变异综合征和L-精氨酸代谢的超级通路。附属组织包括皮肤和脾脏,相关表型包括听力障碍和鼻梁下陷。
Related ID:
MESH:D056732
ICD11:1416203271

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
14
44
33

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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