Williams Syndrome
About the Disease
Williams-Beuren Syndrome, also known as williams syndrome, is related to supravalvular aortic stenosis and williams-beuren region duplication syndrome, and has symptoms including hyperacusis, abnormal weight gain and chronic constipation. An important gene associated with Williams-Beuren Syndrome is ELN (Elastin), and among its related pathways/superpathways is 7q11.23 copy number variation syndrome. The drugs Buspirone and Dopamine have been mentioned in the context of this disorder. Affiliated tissues include heart, bone and eye, and related phenotypes are intellectual disability and hyperreflexia
Common Targets
G85358 | G56979 | G10739 | G1788 | G9752 | G56098 | G22941 | G1859 | G1977 | G29123 | G9759 | G374860 | G9378 | G9423 | G2006 | G4692 | G1804 | G26047 | G9379 | G10988 | G3217 | G5021 | G7681 | G56130 | G5997 | G3201 | G9228 | G22871 | G9369
The "Target / Biomarker Review Report" is a comprehensive and customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about the Target(s) / Biomarker(s) of your choice related to Williams Syndrome, including but not limited to:
• general information;
• protein structure and compound binding;
• protein biological mechanisms;
• its importance;
• the target screening and validation;
• expression level;
• disease relevance;
• drug resistance;
• related combination drugs;
• pharmacochemistry experiments;
• related patent analysis;
• advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai
Other Diseases
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
