| Name | Infantile Neuroaxonal Dystrophy (INAD) Pathway |
| Summary | Comprehensive mechanistic overview of infantile neuroaxonal dystrophy (INAD/PLA2G6-associated neurodegeneration), covering PLA2G6 mutations, axonal transport dysfunction, iron accumulation, and developmental regression |
| Key Genes/Proteins | VPS13C, GENES |
| Related Diseases | Phospholipase A2 Group VI-Associated Neurodegeneration, neurodegeneration, Schizophrenia, Neurodegeneration, Parkinson's disease |
| Related Pathways | demyelination |