Lateral Meningocele Syndrome

About the Disease
Lateral Meningocele Syndrome, also known as lehman syndrome, is related to meningocele and cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1. An important gene associated with Lateral Meningocele Syndrome is NOTCH3 (Notch Receptor 3), and among its related pathways/superpathways are Disease and Signal Transduction. Affiliated tissues include spinal cord, heart and skin, and related phenotypes are ptosis and micrognathia

Common Targets
NOTCH3 | PCYT1A

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