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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
非罕见病
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。
Related ID:
MALACARDS:HMC040
OMIM:236200
MESH:D006712
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
4
173
213
HMC040
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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