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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
Pseudohypoaldosteronism, Type Ib1, Autosomal Recessive (PHA1B1)
Alias:
Autosomal Recessive Pseudohypoaldosteronism Type 1
Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism
Pha1b1
Pha1b
Pseudohypoaldosteronism Type I, Autosomal Recessive
Pseudohypoaldosteronism Type 1 Autosomal Recessive
Pseudohypoaldosteronism 1b1, Autosomal Recessive
Multisystem Pseudohypoaldosteronism
Pha Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type I
Pha I, Autosomal Recessive
Autosomal Recessive Pha 1
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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
伪低醛固酮症,Ib1型,常染色体隐性,也称为常染色体隐性伪低醛固酮症I型,与泛发性伪低醛固酮症I型和伪低醛固酮症I型有关,症状包括腹泻和呕吐。与伪低醛固酮症,Ib1型,常染色体隐性相关的基因是SCNN1A(钠通道上皮1亚单位α),其相关通路/超通路包括无机离子/氨基酸/寡肽和G-βγ信号通路。在该疾病的背景下,已提到的药物有依那普利和依那普利拉。相关组织包括肾脏和肺,相关表型为低血压和脱水。
Related ID:
MALACARDS:PSD122
OMIM:264350
MESH:D011546
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
--
16
147
23
PSD122
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
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No data available
Gene & Mutation
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Gene
Function
Score
Mutations
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Name
CAS Number
Status
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No data available
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Category
Name
MGI
Related Gene
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