Chondrodysplasia Punctata

About the Disease
Chondrodysplasia Punctata Syndrome, also known as chondrodysplasia punctata, is related to x-linked chondrodysplasia punctata 1 and chondrodysplasia punctata 2, x-linked dominant, and has symptoms including edema An important gene associated with Chondrodysplasia Punctata Syndrome is EBP (EBP Cholestenol Delta-Isomerase), and among its related pathways/superpathways are Metabolism and Peroxisomal lipid metabolism. Affiliated tissues include bone, spinal cord and skin, and related phenotypes are no effect and no effect

Common Targets
SIX2 | ARSL | RAF1

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