Pierson Syndrome

About the Disease
Pierson Syndrome, also known as microcoria-congenital nephrotic syndrome, is related to nephrotic syndrome, type 5, with or without ocular abnormalities and nephrotic syndrome, type 1, and has symptoms including edema An important gene associated with Pierson Syndrome is LAMB2 (Laminin Subunit Beta 2), and among its related pathways/superpathways are ERK Signaling and Integrin Pathway. Affiliated tissues include eye, kidney and skeletal muscle, and related phenotypes are hypertension and cataract

Common Targets
LAMB2

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