Spastic Paraplegia 38, Autosomal Dominant (SPG38)

Spastic Paraplegia 38, Autosomal Dominant, also known as spg38, is related to anemia, sideroblastic, and spinocerebellar ataxia and hemochromatosis, type 5. An important gene associated with Spastic Paraplegia 38, Autosomal Dominant is SPG38 (Spastic Paraplegia 38 (Autosomal Dominant, Silver Syndrome)), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Glucose / Energy Metabolism. Affiliated tissues include temporal lobe and spinal cord, and related phenotypes are hyperreflexia and babinski sign