Nephrotic Syndrome

Alias:
Finnish Congenital Nephrotic Syndrome
Glomerular Lesion Nephrosis
Ns - [nephrotic Syndrome]
Nephrosis Syndrome
Nephrosis Nos
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Basic Information
Medical Symptom
Gene & Mutation
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References Literature
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

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Reference
MALACARDS
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Unknown
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150
1356
5

Medical Symptom

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Gene & Mutation

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References Literature

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