Summary

Neurofibromatosis, Familial Spinal, also known as familial spinal neurofibromatosis,is related to neurofibromatosis and watson syndrome,and has symptoms including spinal cord tumor, cafe-au-lait spot and freckling. An important gene associated with Neurofibromatosis, Familial Spinal is NF1 (Neurofibromin 1), and among its related pathways is Glioblastoma Multiforme. Affiliated tissues include spinal cord

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Pathways Associated With Trait

Symptoms Associated With Trait