Nephrotic Syndrome, Type 2 (NPHS2)

Alias:

Nephrotic Syndrome, Steroid-Resistant, Autosomal Recessive

Idiopathic Nephrotic Syndrome

Nephrotic Syndrome Type 2

Nphs2

Srn1

Steroid-Resistant Autosomal Recessive Nephrotic Syndrome

Autosomal Recessive Steroid-Resistant Nephrotic Syndrome

Nephrotic Syndrome, Type 2, Susceptibility to

Nephrotic Syndrome 2

Srn

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Nephrotic Syndrome, Type 2, also known as nephrotic syndrome, steroid-resistant, autosomal recessive, is related to focal segmental glomerulosclerosis and genetic nephrotic syndrome, and has symptoms including edema An important gene associated with Nephrotic Syndrome, Type 2 is NPHS2 (NPHS2 Stomatin Family Member, Podocin), and among its related pathways/superpathways are Primary focal segmental glomerulosclerosis (FSGS) and Markers of kidney cell lineage. The drugs Heptavalent Pneumococcal Conjugate Vaccine and Vaccines have been mentioned in the context of this disorder. Affiliated tissues include kidney and t cells, and related phenotypes are proteinuria and nephrotic syndrome

Related ID：

MALACARDS：NPH049

OMIM：600995

MESH：D009404