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Genetic Diseases, Inborn

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Genetic Diseases, Inborn

Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.

12,573 public trials 2,159 recruiting studies

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Genetic Diseases, Inborn trial results

Recruiting

The United Kingdom National Registry for Myotonic Dystrophy

NCT04003363

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
Locations: John Walton Muscular Dystrophy Research Centre Newcastle upon Tyne, United Kingdom

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Recruiting

The International Registry for Leigh Syndrome

NCT03137355

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +16 more
Locations: The University of Texas Health Science Center at Houston Houston, Texas, United States

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Recruiting

DZHK TORCH-Plus is a Registry for Patients With Cardiomyopathies and Serves as Source for Cardiovascular Research Studies

NCT04265040

Conditions: Amyloidosis, Aortic Stenosis, Subvalvular, Aortic Valve Disease, +25 more
Locations: University Hospital Heidelberg - Clinic of Cardiology, Angiology and Pneumology Heidelberg, Baden-Wurttemberg, Germany

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Longitudinal Observational Study on the Course of Cystic Fibrosis Lung Disease in Patients Following Newborn Screening

NCT02270476

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystic Fibrosis, Cystic Fibrosis Lung Disease, +6 more
Locations: University Children's Hospital Heidelberg, Cystic Fibrosis Centre Heidelberg, Baden-Wurttemberg, Germany

University Hospital Gießen and Marburg GmbH Giessen, Hesse, Germany

Medizinische Hochschule Hannover Hanover, Lower Saxony, Germany

University Children's Hospital Schleswig-Holstein Lübeck, Schleswig-Holstein, Germany

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Recruiting

UTHealth Turner Syndrome Research Registry

NCT03185702

Conditions: Cardiovascular Abnormalities, Cardiovascular Diseases, Chromosome Disorders, +17 more
Locations: University of Texas Health Science Center Houston Houston, Texas, United States

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Multi-model Image of Doxycycline in TAO

NCT05112211

Conditions: Autoimmune Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, +12 more
Locations: Zhongshan Ophthalmic Center Guangzhou, Guangdong, China

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ADPKD Patient Registry

NCT04039061

Conditions: Abnormalities, Multiple, Ciliopathies, Congenital Abnormalities, +10 more
Locations: PKD Foundation Kansas City, Missouri, United States

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Biomarkers and Cardiac Imaging Diagnostic Assay for Monitoring Patients With Fabry Disease

NCT05698901

Conditions: Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +23 more
Locations: Charles Jia-Yin Hou Taipei, Taiwan

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Recruiting

Cardiac Amyloidosis Registry of University Hospital Leipzig

NCT06129656

Conditions: Amyloid Neuropathies, Amyloid Neuropathies, Familial, Amyloidosis, +18 more
Locations: University Hospital Leipzig Leipzig, Saxony, Germany

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Halting Ornithine Transcarbamylase Deficiency With Recombinant AAV in ChildrEn

NCT05092685

Conditions: Amino Acid Metabolism, Inborn Errors, Brain Diseases, Brain Diseases, Metabolic, +12 more
Locations: Great Ormond Street Hospital London, United Kingdom

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Genetic Diseases, Inborn

Genetic Diseases, Inborn trial results

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