Deafness, Autosomal Dominant 82 (DFNA82)

Alias:
Dfna82
Hearing Loss, Autosomal Dominant 82
Deafness, Autosomal Dominant, 82
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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
听觉障碍,常染色体显性82,也被称为dfna82。与听觉障碍,常染色体显性82有关的重要基因是ATP2B2(ATPase Plasma Membrane Ca2+ Transporting 2)。相关组织包括大脑,相关表型包括感觉神经性听力障碍和耳鸣。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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1
19
4

Medical Symptom

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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
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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