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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
非罕见病
Meniere Disease
Alias:
Meniere's Disease
Ménière's Disease
Otogenic Vertigo
Ménière Disease
Idiopathic Endolymphatic Hydrops
Primary Endolymphatic Hydrops
Labyrinthine Hydrops
Labyrinthine Vertigo
Meniere's Syndrome
Ménière's Vertigo
Labyrinth Hydrops
Auditory Vertigo
Menieres Disease
Ménière Syndrome
Mnire's Vertigo
Ménière Vertigo
Vertigo, Aural
Aural Vertigo
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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
梅尼埃病,又称梅尼埃病,与耳硬化症和迷路炎有关,症状包括咳嗽、打鼾和耳鸣。与梅尼埃病有关的重要基因是FAM136A(序列相似性136家族成员A)。在该疾病的背景下提到了孟鲁司特和柠檬酸钠。附属组织包括骨和脑,相关表型为听力障碍和眩晕
Related ID:
MALACARDS:MNR012
OMIM:156000
MESH:D008575
ICD11:683932278
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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26
241
12
MNR012
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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