Nephrotic Syndrome

Alias:
Finnish Congenital Nephrotic Syndrome
Glomerular Lesion Nephrosis
Ns - [nephrotic Syndrome]
Nephrosis Syndrome
Nephrosis Nos
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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
Nephrotic Syndrome, also known as Finnish congenital nephrotic syndrome, is related to familial nephrotic syndrome and genetic steroid-resistant nephrotic syndrome, and has symptoms including edema. An important gene associated with Nephrotic Syndrome is NPHS2 (NPHS2 Stomatin Family Member, Podocin), and among its related pathways/superpathways are Signal Transduction and Non-integrin membrane-ECM interactions. The drugs Entecavir and Acetazolamide have been mentioned in the context of this disorder. Affiliated tissues include kidney and pituitary, and related phenotypes are renal/urinary system and homeostasis/metabolism.
Related ID:
MESH:D009404
ICD11:1184209951

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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150
1356
5

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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No Data Found!
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