Mapping the Genotype, Phenotype, and Natural History of Phelan-McDermid Syndrome | ClinicalTrials HQ

Ask about research services

Swipe the table sideways for more columns.

Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Mapping the Genotype, Phenotype, and Natural History of Phelan-McDermid Syndrome	Neurobehavioral Manifestations, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Phelan-McDermid syndrome, Signs and Symptoms, autism spectrum disorder, intellectual disability, nervous system disorder, neurodevelopmental disorder, pervasive developmental disorder, psychiatric disorder	Active, not recruiting	Not stated	2026-08-06		NCT02461420

7 results · Page 1 of 1

Swipe the table sideways for more columns.

Organizations	Linked trials
Boston Children's Hospital	238
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)	536
National Center for Advancing Translational Sciences (NCATS)	127
National Institute of Neurological Disorders and Stroke (NINDS)	370
National Institutes of Health (NIH)	667
Office of Rare Diseases (ORD)	7
Phelan-McDermid Syndrome Foundation	1

5 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sites	City	Country	Linked trials
Boston Children's Hospital	Boston	United States	343
Icahn School of Medicine at Mount Sinai	New York	United States	342
National Institutes of Health	Bethesda	United States	10
Rush University Medical Center	Chicago	United States	283
Stanford University	Stanford	United States	213