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Clinical trial condition

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

Czech AATD Registry

NCT05178277

Conditions
Alpha-1-antitrypsin Deficiency, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, +9 more
Locations
  • Thomayer university hospital Prague, Czech Republic, Czechia
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Recruiting

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

NCT01403402

Conditions
Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations), Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy), Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan), +89 more
Locations
  • Congenital Muscle Disease International Registry (www.cmdir.org) Lakewood, California, United States
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Recruiting

Long-Term Follow-up Protocol

NCT04917887

Conditions
Collagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +12 more
Locations
  • Mission Dermatology Center Rancho Santa Margarita, California, United States
  • Stanford University Redwood City, California, United States
  • Pediatric Skin Research Coral Gables, Florida, United States
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Recruiting

Phenotypes, Biomarkers and Pathophysiology in Hereditary Spastic Paraplegias and Related Disorders

NCT03981276

Conditions
Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +10 more
Locations
  • University Innsbruck Innsbruck, Austria
  • German Center for Neurodegenerative Diseases (DZNE) Bonn Bonn, Germany
  • University of Erlangen Erlangen, Germany
  • University Medicine Essen Essen, Germany
View all 13 locations
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