Wolfram Syndrome 2
About the Disease
Wolfram Syndrome 2, also known as wfs2, is related to optic nerve disease and wolfram syndrome. An important gene associated with Wolfram Syndrome 2 is CISD2 (CDGSH Iron Sulfur Domain 2), and among its related pathways/superpathways are Immune response Function of MEF2 in T lymphocytes and Neuroscience. Affiliated tissues include bone marrow, bone and skeletal muscle, and related phenotypes are gastric ulcer and diabetes mellitus
Common Targets / Biomarkers
G493856
Other Diseases
Wolman Disease | Woodhouse-Sakati Syndrome | X-linked Acrogigantism | X-linked Charcot-Marie-Tooth Disease | X-linked Creatine Transporter Deficiency | X-linked Myotubular Myopathy | X-linked Sideroblastic Anemia | Xeroderma Pigmentosum | Xeroderma Pigmentosum Variant Type | Yellow Fever | Zellweger Syndrome | Zimmermann-Laband Syndrome | Zollinger-Ellison Syndrome | Zygomycosis
