Wieacker-Wolff Syndrome
About the Disease
Wieacker-Wolff Syndrome, also known as wieacker syndrome, is related to wieacker-wolff syndrome, female-restricted and miles-carpenter syndrome, and has symptoms including apnea, muscle spasticity and ophthalmoplegia. An important gene associated with Wieacker-Wolff Syndrome is ZC4H2 (Zinc Finger C4H2-Type Containing). Affiliated tissues include tongue, eye and brain, and related phenotypes are neurological speech impairment and global developmental delay
Common Targets / Biomarkers
G8824 | G10869 | G55906 | G54658 | G5406
Other Diseases
Wiedemann-Steiner Syndrome | 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
