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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
Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency (DHFRD)
Alias:
Constitutional Megaloblastic Anemia with Severe Neurologic Disease
Dhfr Deficiency
Dihydrofolate Reductase Deficiency
Anemia, Megaloblastic, Due to Dihydrofolate Reductase Deficiency
Deficiency of Dihydrofolate Reductase
Dhfrd
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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
巨幼细胞性贫血由于二氢叶酸还原酶缺乏症,也称为伴有严重神经疾病的遗传性巨幼细胞性贫血,与巨幼细胞性贫血和转钴胺素ii缺乏症有关,症状包括共济失调、黄疸和失神发作。与巨幼细胞性贫血由于二氢叶酸还原酶缺乏症相关的重要基因是DHFR(二氢叶酸还原酶)。相关组织包括骨髓和骨,相关表型为平均血小板体积增加和CSF 5-甲基四氢叶酸浓度降低。
Related ID:
MALACARDS:MGL012
OMIM:613839
MESH:D000749
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
婴儿期
<1/1000000
1
7
5
MGL012
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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