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NPHS1

—NPHS1 Adhesion Molecule Nephrin

Chromosome: 19

Location: 19:35825372-35869287

OMIM: 602716

Ensembl: ENSG00000161270

Official·OMIM:602716 Official·ENSG00000161270

Encodes nephrin protein. Mutations cause congenital nephrotic syndrome.

Treatment Roadmap — NPHS1

Preclinical

Phase 1

Phase 2

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Congenital Nephrotic Syndrome

Autosomal RecessivePrevalence: 1/50000renal

Official·OMIM:256300 Official·ORPHA839

Summary

Clinical Trial

Approved Therapy

Registered Variant