National Human Genome Research Institute (NHGRI): Genetic Diseases, Inborn trials

The registry lists 10 Genetic Diseases, Inborn studies with National Human Genome Research Institute (NHGRI) as lead sponsor. 3 are open to participants now and 0 have results posted.

No phase 10(a study in two phases counts in both)

Studies

Open to participants first, then studies with results posted, then the rest; newest registration first within each.

• Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases NetworkRecruitingNCT02450851
• Genome Medical Sequencing for Gene DiscoveryRecruitingNCT01087320
• Familial Mediterranean Fever and Related Disorders: Genetics and Disease CharacteristicsRecruitingNCT00001373
• Insights Into Microbiome and Environmental Contributions to Sickle Cell Disease and Leg Ulcers Study (INSIGHTS Study)CompletedNCT02156102
• Inherited Diseases, Caregiving, and Social NetworksCompletedNCT01498263
• The Role of Family Functioning in Promoting Adaptation in Siblings of Individuals With Duchenne Muscular Dystrophy (DMD)TerminatedNCT01386515
• Personalized Genomic ResearchCompletedNCT01294345
• Genetic Studies in the Amish and MennonitesCompletedNCT00359580
• Microarray Analysis for Human Genetic DiseaseCompletedNCT00001898
• Study of Clinical and Molecular Manifestations of Genetic DisordersCompletedNCT00001466