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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
罕见病
Hypertension, Essential (EHT)
Alias:
Essential Hypertension
Hypertension
High Blood Pressure
Hypertension, Essential, Susceptibility to
Hypertensive Disease
Primary Hypertension
Hypertension, Salt-Sensitive Essential, Susceptibility to
Idiopathic Hypertension
Hypertensive Disorder
Hyperpiesia
Eht
Hypertension, Essential, Susceptibility to, 1
Hypertension, Essential, Susceptibility to, 2
Hypertension, Essential, Susceptibility to, 3
Hypertension, Essential, Susceptibility to, 4
Hypertension, Essential, Susceptibility to, 5
Hypertension, Essential, Susceptibility to, 6
Hypertension, Essential, Salt-Sensitive
Systemic Arterial Hypertensive Disorder
Hypertension, Salt-Sensitive Essential
Systemic Primary Arterial Hypertension
Hypertensive Vascular Degeneration
Hypertension, Susceptibility to
Essential Hypertension, Genetic
Vascular Hypertensive Disorder
Systemic Arterial Hypertension
Hypertensive Vascular Disease
Primary Htn - [hypertension]
High Blood Pressure Disorder
Hbp - [high Blood Pressure]
Cardiovascular Hypertension
Hypertension, Essential 1
Hypertension, Essential 2
Hypertension, Essential 3
Hypertension, Essential 4
Hypertension, Essential 5
Hypertension, Essential 6
Arterial Hypertension Nos
Cholesterol Hypertension
Elevated Blood Pressure
Malignant Hypertension
Systemic Hypertension
Vascular Hypertension
Raised Blood Pressure
High Arterial Tension
Htn - [hypertension]
Benign Hypertension
Ht - [hypertension]
Hypertension Nos
Cholesterol Htn
Idiopathic Htn
Malignant Htn
Vascular Htn
Artery Htn
Benign Htn
Htn
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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
高血压,原发性,又称原发性高血压,与肺动脉高压和肾血管性高血压有关,症状包括心绞痛、胸痛和水肿。与原发性高血压相关的基因是AGTR1(血管紧张素II受体1),其相关通路/超级通路包括发育血管紧张素激活ERK和促肾上腺皮质激素释放激素信号通路。在该疾病的背景下,已提到的药物包括卡那洛酸和顺阿曲库铵。附属组织包括心脏和肾脏,相关表型为收缩压升高和舒张压升高。
Related ID:
MALACARDS:HYP595
OMIM:145500
MESH:D000075222
ICD11:761947693
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
未知
--
439
5032
128
HYP595
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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