Hermansky-Pudlak Syndrome 1 (HPS1)

Alias:
Albinism with Hemorrhagic Diathesis and Pigmented Reticuloendothelial Cells
Hps1
Delta Storage Pool Disease
Albinism with Hemorrhagic Diathesis and Pigmented Reticuloendothelial
Hermansky-Pudlak Syndrome, Type 1
Platelet Storage Pool Deficiency
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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
赫曼斯基-普德拉克综合症1,也称为出血性素质和色素性网状内皮细胞的白化病,与肺纤维化和赫曼斯基-普德拉克综合症6有关,症状包括腹痛。与赫曼斯基-普德拉克综合症1有关的重要基因是HPS1(HPS1生物合成溶酶体器官复合物3亚基1),其相关通路/超通路包括跨高尔基体网络囊泡芽生。在该疾病的背景下提到了药物吡非尼酮和普拉伐他汀。附属组织包括肺和皮肤,相关表型为眼震和畏光。
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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

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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