Example: Heart Attack

Clinical Trials on Genetic Diseases, Inborn

Total 10334 results

    • NCT03721458
      Completed
      Whole Genome Sequencing in the Neonatal Intensive Care Unit
      Conditions: Genetic Diseases, Inborn
    • NCT03587155
      Unknown status
      Study on the Mechanism of Neurodevelopment Dysplasia of Fetal Brain Caused by ASNS Gene Mutation
      Conditions: Asparagine Synthetase Deficiency; Genetic Diseases, Inborn
    • NCT02676479
      Unknown status
      Uterine Irrigation Method in Infertility Patients Who Require PGD
      Conditions: Pre-Implantation Embryo Recovery; Genetic Diseases, Inborn
    • NCT03738098
      Active, not recruiting
      NYCKidSeq: Incorporating Genomics Into Clinical Care of Diverse NYC Children
      Conditions: Genetic Diseases, Inborn; Genetic Predisposition to Disease
    • NCT02884063
      Completed
      Utilizing Free DNA in Embryo Culture for PGS
      Conditions: Chromosome Abnormalities; Genetic Diseases, Inborn; Mutation
    • NCT00458055
      Completed
      High-Density Lipoprotein (HDL) Treatment Study
      Conditions: Coronary Arteriosclerosis; Hypoalphalipoproteinemias; Genetic Diseases, Inborn
    • NCT02225522
      Completed
      Genomic Sequencing in Acutely Ill Neonates
      Conditions: Diseases/Diagnoses; Genetic Disease
    • NCT02921321
      Recruiting
      Pilot Study of Cardiac MR in Patients With Muscular Dystrophy
      Conditions: Muscular Dystrophies; Cardiac Fibrosis; Genetic Diseases, Inborn; Musculoskeletal Diseases
    • NCT00288704
      Completed
      Rilonacept for Treatment of Cryopyrin-Associated Periodic Syndromes (CAPS)
      Conditions: Familial Cold Autoinflammatory Syndrome (FCAS); Familial Cold Urticaria; Muckle-Wells Syndrome (MWS); Genetic Diseases, Inborn
    • NCT03612310
      Not yet recruiting
      Developing Protocols for Modelling of Genetic Diseases Using Induced Pluripotent Stem Cells
      Conditions: Genetic Disease
    • NCT02380729
      Completed
      Mutation Exploration in Non-acquired, Genetic Disorders and Its Impact on Health Economy and Life Quality
      Conditions: Genetic Diseases
    • NCT03971292
      Not yet recruiting
      Interest of High-throughput Sequencing of RNAs for the Diagnosis of Heterogeneous Genetic Diseases
      Conditions: DNA Sequencing; Diagnosis of Genetic Diseases of Heterogeneous Origin
    • NCT04248504
      Not yet recruiting
      Digital Genetic Assistant (DGA) for Expanded Carrier Screening
      Conditions: Genetic Disease
    • NCT04014114
      Not yet recruiting
      The Use of Digital Genetic Assistant (DGA) for Expanded Carrier Screening
      Conditions: Genetic Disease
    • NCT02450851
      Recruiting
      Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
      Conditions: Genetic Disease
    • NCT03658382
      Withdrawn
      Virtual Visits for Results Disclosure
      Conditions: Genetic Disease
    • NCT04183023
      Not yet recruiting
      Population Genomic Diversity of France
      Conditions: Genetic Disease
    • NCT03458962
      Enrolling by invitation
      Diagnostic Odyssey: Whole Genome Sequencing (WGS)
      Conditions: Genetic Disease; Genetic Syndrome
    • NCT02266615
      Recruiting
      Biobank Clinical Genetics Maastricht (KG01)
      Conditions: Genetic Disease
    • NCT00705055
      Completed
      Face Anthropometric Pattern Recognition Technology for Computer Aided Diagnosis of Human Genetic Disorders.
      Conditions: Genetic Disorders
    • NCT03084224
      Recruiting
      Implementation of Molecular Diagnostic Pathways
      Conditions: Genetic Disease
    • NCT03918707
      Recruiting
      Utility of Rapid Whole Genome Sequencing in the NICU: A Pilot Study
      Conditions: Genetic Disease; Genetic Syndrome
    • NCT02917460
      Recruiting
      Rady Children's Institute Genomic Biorepository
      Conditions: Genetic Diseases
    • NCT03385876
      Enrolling by invitation
      Rapid Whole Genome Sequencing Study
      Conditions: Genetic Diseases; Genetic Syndrome
    • NCT03211039
      Active, not recruiting
      Perinatal Precision Medicine
      Conditions: Genetic Diseases; Genetic Syndrome
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