Mowat-Wilson syndrome due to monosomy 2q22 is a rare condition that has been described with several different names, including Hirschsprung disease and intellectual disability due to 2q22 microdeletion and other similar terms. These synonyms hint that the condition may include problems with the intestines, such as those seen in Hirschsprung disease, as well as challenges with learning or intellectual development. The understanding of this condition is still in early stages. Detailed information about its causes, progression, and full clinical picture is currently limited. Further research is needed to better understand how changes in the 2q22 region of the chromosome lead to the symptoms seen in people with this disorder.

Information about symptoms is currently limited for this condition.

Information about causes is currently limited for this condition.