Smith-Lemli-Opitz Syndrome (SLOS)

Alias:
Slos
7-Dehydrocholesterol Reductase Deficiency
Rsh Syndrome
Rutledge Lethal Multiple Congenital Anomaly Syndrome
Slo Syndrome
Polydactyly, Sex Reversal, Renal Hypoplasia, and Unilobar Lung
Smith-Lemli-Opitz Syndrome, Type Ii
Lethal Acrodysgenital Syndrome
Smith-Opitz-Inborn Syndrome
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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
史密斯-莱姆利-奥普茨综合症,也被称为slos,与格林伯格发育不良和家族性高胆固醇血症1有关,其症状包括便秘、癫痫发作和呕吐。与史密斯-莱姆利-奥普茨综合症有关的重要基因是DHCR7(7-脱氢胆固醇还原酶),其相关通路/超级通路包括代谢和葡萄糖/能量代谢。在该疾病的背景下提到了辛伐他汀和苯佐卡因。附属组织包括肺和眼,相关表型为智力障碍和肌张力低下。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
1-9/100000
37
419
227

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

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
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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