Homocystinuria Due to Cystathionine Beta-Synthase Deficiency (CBSD)

Alias:
Homocystinuria with or Without Response to Pyridoxine
Homocystinuria, B6-Responsive and Nonresponsive Types
Hyperhomocysteinemia, Thrombotic, Cbs-Related
Cystathionine Beta-Synthase Deficiency
Cbs Deficiency
Homocystinuria Due to Cystathionine Beta-Synthase
Cystathionine Beta-Synthase Deficiency Disease
Hyperhomocysteinemia Thrombotic Cbs-Related
Thrombosis, Hyperhomocysteinemic
Homocystinuria, Cbs Deficiency
Classic Homocystinuria
Cbsd
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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
同型半胱氨酸尿症,由于半胱氨酸β-合成酶缺乏,也称为对或不对吡哆醇有反应的同型半胱氨酸尿症,与半胱氨酸β-合成酶缺乏引起的同型半胱氨酸尿症和同型半胱氨酸尿症有关,症状包括癫痫发作。与同型半胱氨酸尿症,由于半胱氨酸β-合成酶缺乏有关的重要基因是CBS(半胱氨酸β-合成酶)。在该疾病的背景下,已提到的药物包括对乙酰氨基酚和乙酰半胱氨酸。附属组织包括皮肤和肝脏,相关表型为生长发育迟缓和晶状体脱位。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
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Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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