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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
Hyperferritinemia with or Without Cataract (HRFTC)
Alias:
Hyperferritinemia-Cataract Syndrome
Hereditary Hyperferritinemia with Congenital Cataracts
Hhcs
Hyperferritinemia, Hereditary, with Congenital Cataracts
Hereditary Hyperferritinemia-Cataract Syndrome
Bonneau-Beaumont Syndrome
Hrftc
Cataract-Hyperferritinemia Syndrome
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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
铁蛋白过高伴有或不伴有白内障,也称为铁蛋白过高-白内障综合症,与神经退行性脑铁沉积3和铁代谢疾病有关。与铁蛋白过高伴有或不伴有白内障相关的基因是FTL(铁蛋白轻链),其相关通路/超级通路包括无机离子/酸的运输和氨基酸/寡肽和葡萄糖/能量代谢。附属组织包括眼睛和肝脏,相关表型为白内障和代谢/稳态异常。
Related ID:
MALACARDS:HYP801
OMIM:600886
MESH:C538137
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
全年龄段
<1/1000000
14
144
44
HYP801
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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