Neurologic, Endocrine, and Pancreatic Disease, Multisystem, Infantile-Onset 1 (IMNEPD1)

Alias:
Neurologic, Endocrine, and Pancreatic Disease, Multisystem, Infantile-Onset
Imnepd
Imnepd1
Multisystem Neurologic, Endocrine, and Pancreatic Disease, Infantile-Onset
Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease
Infantile Multisystem Neurologic-Endocrine-Pancreatic Disease
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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
神经内分泌胰腺疾病,多系统,婴儿型1,也称为神经内分泌胰腺疾病,多系统,婴儿型,与神经内分泌胰腺疾病,多系统,婴儿型2和感觉神经性听力损失有关,症状包括共济失调。与神经内分泌胰腺疾病,多系统,婴儿型1相关的基因是PTRH2(肽基-TRNA水解酶2)。相关组织包括大脑和胰腺,相关表型为共济失调和全球发育延迟。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
婴儿期
<1/1000000
3
11
7

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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