This website provides information on patients with mutations in the IL1RAPL1 (interleukin 1 receptor accessory protein like 1) gene, including clinical data, molecular data, management and research options.

Mutations and deletions of the interleukin-1 receptor accessory protein like 1 (IL1RAPL1) gene, are associated with X-linked non-syndromic intellectual disability (ID) and autism spectrum disorders (ASD).

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the IL1RAPL1 gene.

Carlo Sala, MD, PhD, CNR Neuroscience Institute, Milano, Vedano al Lambro, Italy, carlo.sala@in.cnr.it