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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
Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity (MTHFRD)
Alias:
Methylenetetrahydrofolate Reductase Deficiency
Mthfr Deficiency
Homocystinuria Due to Methylene Tetrahydrofolate Reductase Deficiency
Homocystinuria Due to Mthfr Deficiency
Methylene Tetrahydrofolate Reductase Deficiency
5,10-Methylenetetrahydrofolate Reductase Deficiency
Homocysteinemia, Due to Deficiency of Mthfr
Mthfrd
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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
N-甲基四氢叶酸还原酶活性缺乏引起的高同型半胱氨酸血症和同型半胱氨酸血症,也称为甲硫氨酸四氢叶酸还原酶缺乏症,症状包括癫痫发作、肌肉无力和肌肉痉挛。与N-甲基四氢叶酸还原酶活性缺乏引起的高同型半胱氨酸血症相关的基因是MTHFR(甲硫氨酸四氢叶酸还原酶),其相关通路/超级通路包括水溶性维生素和辅因子代谢、一碳代谢和相关通路。相关组织包括脊髓和大脑,相关表型为步态障碍和上运动神经元功能障碍。
Related ID:
MALACARDS:HMC041
OMIM:236250
MESH:D006712
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
--
2
11
98
HMC041
Medical Symptom
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Description
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Orphanet Frequency
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No data available
Gene & Mutation
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