Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant, also known as adult-onset autosomal dominant demyelinating leukodystrophy, is related to autosomal dominant leukodystrophy with autonomic disease and lmnb1-related autosomal dominant leukodystrophy, and has symptoms including cerebellar ataxia, muscle spasticity and abnormal pyramidal signs. An important gene associated with Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant is LMNB1 (Lamin B1), and among its related pathways/superpathways are DREAM Repression and Dynorphin Expression and Cytoskeletal Signaling. Affiliated tissues include eye and spinal cord, and related phenotypes are ataxia and abnormal autonomic nervous system physiology