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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
Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency (DRDSPRD)
Alias:
Sepiapterin Reductase Deficiency
Spr Deficiency
Dopa-Responsive Dystonia Due to Sepiapterin Reductase Deficiency
Drd Due to Srd
Autosomal Recessive Sepiapterin Reductase-Deficient Drd
Srd
Motor and Cognitive Disorder Due to Sepiapterin Reductase Deficiency
Dopa-Responsive Hypersomnia
Psychomotor Disorders
Dyt-Spr
Drdsprd
Spr
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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
肌张力障碍-多巴反应性,由于色氨酸生物合成酶缺乏症,也称为色氨酸生物合成酶缺乏症,与高苯丙氨酸血症、Bh4缺乏症、A型和节段性肌张力障碍有关,症状包括嗜睡、神经行为表现和精神运动技能受损。与肌张力障碍-多巴反应性,由于色氨酸生物合成酶缺乏症相关的基因是SPR(色氨酸生物合成酶),其相关通路/超通路包括代谢和SLITs和ROBOs的表达调控。在该疾病的背景下,已提到的药物有佐匹克隆和阿普唑仑。相关组织包括眼和甲状腺,相关表型为智力障碍和高反射。
Related ID:
MALACARDS:DYS161
OMIM:612716
MESH:C562657
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
20
170
17
DYS161
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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