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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
Glutamate Formiminotransferase Deficiency (FIGLU-URIA)
Alias:
Formiminoglutamic Aciduria
Formiminotransferase Cyclodeaminase Deficiency
Formiminotransferase Deficiency
Ftcd Deficiency
Figlu-Uria
Arakawa Syndrome 1
Formiminotransferase Deficiency Syndrome
Formiminoglutamic Acidemia
Formiminoglutamicaciduria
Figluria
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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
谷氨酸-5-甲酰胺转移酶缺乏症,也称为5-甲酰胺-谷氨酸尿症,与高半胱氨酸尿症和巨幼细胞性贫血有关。与谷氨酸-5-甲酰胺转移酶缺乏症相关的基因是FTCD(5-甲酰胺转移酶环氧化酶),其相关通路/超级通路包括代谢和SLITs和ROBOs的表达调控。相关组织包括皮肤和中性粒细胞,相关表型包括循环组氨酸浓度异常和叶酸代谢异常。
Related ID:
MALACARDS:GLT005
OMIM:229100
MESH:C537425
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
孩童期
--
14
71
14
GLT005
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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