Cholestasis, Progressive Familial Intrahepatic, 1 (PFIC1)

Alias:
Byler Disease
Pfic1
Progressive Familial Intrahepatic Cholestasis Type 1
Cholestasis, Progressive Familial Intrahepatic 1
Fic1 Deficiency
Progressive Familial Intrahepatic Cholestasis 1
Cholestasis, Intrahepatic, Familial, Progressive, Type 1
Cholestasis, Progressive Familial Intrahepatic 3
Progressive Intrahepatic Cholestasis
Fatal Intrahepatic Cholestasis
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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
胆汁淤积症,家族性进行性肝内型1,也称为Byler病,与胆汁淤积症,家族性进行性肝内型5和胆汁淤积症,家族性进行性肝内型2有关,其症状包括腹泻、黄疸和瘙痒。与胆汁淤积症,家族性进行性肝内型1有关的重要基因是ATP8B1(ATPase Phospholipid Transporting 8B1),其相关通路/超级通路包括无机离子/氨基酸/寡肽的运输和心脏传导。在该疾病的背景下,已提到的药物包括胆汁酸和盐以及苯丙酸。相关组织包括肝脏和肺,相关表型为黄疸和结合性高胆红素血症。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
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36
194
46

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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