Deafness, Autosomal Dominant 25 (DFNA25)

Alias:
Dfna25
Autosomal Dominant Nonsyndromic Deafness 25
Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 25
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 25
Autosomal Dominant Nonsyndromic Hearing Loss 25
Deafness, Autosomal Dominant, Type 25
Deafness, Autosomal Dominant, 25
Autosomal Dominant Deafness 25
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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25型,也称为dfna25,与非综合征性听力损失和感觉神经性听力损失有关。与听觉障碍,常染色体显性25型有关的重要基因是SLC17A8(溶质载体家族17成员8),其相关通路/超级通路包括嗅觉信号通路和纤毛景观。相关组织包括大脑,相关表型包括感觉神经性听力障碍和异常前庭功能。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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15
202
6

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

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CAS Number
Status
Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
No Data Found!
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