Nephrotic Syndrome, Type 1 (NPHS1)

Alias:

Finnish Congenital Nephrosis

Finnish Congenital Nephrotic Syndrome

Nphs1

Congenital Nephrotic Syndrome, Finnish Type

Congenital Nephrotic Syndrome

Nephrotic Syndrome Type 1

Cnf

Congenital Nephrotic Syndrome of the Finnish Type

Nephrotic Syndrome, Congenital

Nephrosis, Congenital

Nephrotic Syndrome 1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Nephrotic Syndrome, Type 1, also known as finnish congenital nephrosis, is related to nephrotic syndrome, type 2 and focal segmental glomerulosclerosis 1, and has symptoms including edema An important gene associated with Nephrotic Syndrome, Type 1 is NPHS1 (NPHS1 Adhesion Molecule, Nephrin), and among its related pathways/superpathways are Cell junction organization and Primary focal segmental glomerulosclerosis (FSGS). Affiliated tissues include kidney and placenta, and related phenotypes are proteinuria and abnormal renal tubule morphology

Related ID：

MALACARDS：NPH055

OMIM：256300

MESH：D009404