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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
Hemochromatosis, Type 4 (HFE4)
Alias:
Hemochromatosis Type 4
Hemochromatosis Due to Defect in Ferroportin
Ferroportin Disease
Hfe4
Autosomal Dominant Hereditary Hemochromatosis
Hemochromatosis, Autosomal Dominant
Hemochromatosis Autosomal Dominant
Slc40a1-Related Hemochromatosis
Hemochromatosis 4
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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
血色素沉着症4型,也称为血色素沉着症4型,与HJV或HAMP相关的血色素沉着症和血色素沉着症5型有关,其症状包括关节痛和疲劳。与血色素沉着症4型有关的重要基因是SLC40A1(溶质载体家族40成员1),其相关通路/超级通路包括无机离子/阴离子和氨基酸/寡肽的运输以及胰岛素受体回收。在该疾病的背景下提到了铁和Hepcidins药物。附属组织包括肝脏和心脏,相关表型为循环铁蛋白浓度增加和肝脂肪变性。
Related ID:
MALACARDS:HMC035
OMIM:606069
MESH:C537249
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
全年龄段
--
14
144
40
HMC035
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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