Wiedemann-Steiner Syndrome
About the Disease
Wiedemann-Steiner Syndrome, also known as wdsts, is related to hypertrichosis and kabuki syndrome 1. An important gene associated with Wiedemann-Steiner Syndrome is KMT2A (Lysine Methyltransferase 2A), and among its related pathways/superpathways are DNA IR-double strand breaks and cellular response via ATM and Chromatin Regulation / Acetylation. Affiliated tissues include eye and bone, and related phenotypes are delayed speech and language development and dysphagia
Common Targets / Biomarkers
G4297
Other Diseases
Williams Syndrome | Wilson's Disease | Wiskott-Aldrich Syndrome | Withdrawal Syndrome | Wolcott-Rallison Syndrome | Wolff-Parkinson-White Syndrome | Wolfram Syndrome | Wolfram Syndrome 2 | 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
