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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
Urocanase Deficiency (UROCD)
Alias:
Encephalopathy Due to Urocanase Deficiency
Urocanic Aciduria
Urocanate Hydratase Deficiency
Urocd
High Urine Urocanic Acid Levels
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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
尿苷二磷酸尿苷酶缺乏症,也称为尿苷二磷酸尿苷酶缺乏症性脑病,与组氨酸血症和组氨酸代谢疾病有关,症状包括共济失调和震颤。与尿苷二磷酸尿苷酶缺乏症相关的基因是UROC1(尿苷二磷酸尿苷酶1),其相关通路/超级通路包括组氨酸降解。相关组织包括肝脏,相关表型包括共济失调和言语不清。
Related ID:
MALACARDS:URC006
OMIM:276880
MESH:C536479
ICD11:61773927
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
11
53
3
URC006
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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