You are using an outdated browser. Please upgrade your browser to improve your experience.
6q16 deletion syndrome
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Deletion 6q16 syndrome is a Prader-Willi like syndrome characterized by obesity, hyperphagia, hypotonia, small hands and feet, eye/vision anomalies, and global developmental delay.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:171829
UMLS:CN200301
MONDO:0015749
High level summary of knowledge for a disease, including descriptions and datasource references.