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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
Cholestasis, Progressive Familial Intrahepatic, 2 (PFIC2)
Alias:
Pfic2
Progressive Familial Intrahepatic Cholestasis Type 2
Cholestasis, Progressive Familial Intrahepatic 2
Bsep Deficiency
Progressive Familial Intrahepatic Cholestasis 2
Cholestasis, Intrahepatic, Familial, Progressive, Type 2
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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,2型,也称为pfic2,与家族性肝内胆汁淤积和胆道闭锁有关,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,2型有关的重要基因是ABCB11(ATP结合盒家族B成员11),其相关通路/超通路包括无机离子/氨基酸/寡肽的代谢和运输。在该疾病的背景下提到了胆汁酸和盐类药物。相关组织包括肝脏和脾脏,相关表型为生长发育不良和脾肿大。
Related ID:
MALACARDS:CHL136
OMIM:601847
MESH:C535934
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
--
23
128
22
CHL136
Medical Symptom
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Description
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Gene & Mutation
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