Page 1 of Clinical Trials for "Genetic Diseases, Inborn", 3579 Total Matches
- 1CompletedLast Updated: December 1, 2011Condition(s): Familial Cold Autoinflammatory Syndrome (FCAS); Familial Cold Urticaria; Muckle-Wells Syndrome (MWS); Genetic Diseases, Inborn
- 2Active, not recruitingLast Updated: January 17, 2012Condition(s): Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
- 3CompletedLast Updated: June 2, 2008Condition(s): Coronary Arteriosclerosis; Hypoalphalipoproteinemias; Genetic Diseases, Inborn
- 4CompletedLast Updated: October 2, 2010Condition(s): Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
- 5CompletedLast Updated: February 1, 2011Condition(s): Lipid Metabolism, Inborn Errors; Hyperlipidemias; Metabolic Diseases; Hypolipoproteinemia; Hypolipoproteinemias; Hypobetalipoproteinemias; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Congenital Abnormalities; Metabolic Disorder; Hypercholesterolemia; Dyslipidemias; Lipid Metabolism Disorders
- 6CompletedLast Updated: January 18, 2012Condition(s): Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
- 7RecruitingLast Updated: March 20, 2012Condition(s): Inborn Genetic Diseases; Pentalogy of Cantrell
- 8RecruitingLast Updated: July 28, 2011Condition(s): Muscular Dystrophy; Congenital Muscular Dystrophy; Fukutin-related Protein Gene; Limb Girdle; FKRP Gene; Childhood Onset LGMD; Adult Onset LGMD; POMT1; POMT2; POMGnT1; LARGE; Alpha Dystroglycan; Dystroglycanopathy; Centronuclear; Multiminicore; Multicore; Minicore; Congenital Fiber Type Disproportion; Myotubular; Nemaline; Congenital Myopathy; Neuromuscular; Rigid Spine; Phenotype-Genotype Correlation; Cough Assisted Device; Neuromuscular Disease; Respiratory Exacerbation; Invasive Ventilation; Chest Physiotherapy; Congenital Myopathies; Genetic Mutations; Hypertrophic Cardiomyopathy; Wheelchair Use; Cataract; Opthalmoplegia; Ullrich Congenital Muscular Dystrophy; Intermediate Collagen VI Myopathy; Laminin Alpha 2 Related Congenital Muscular Dystrophy; MDC1A; Merosin Deficient Congenital Muscular Dystrophy; Congenital Muscular Dystrophy Undiagnosed; Congenital Muscular Dystrophy Merosin Positive; Walker Warburg Syndrome; Muscle Eye Brain Disease; Fukuyama; Integrin Alpha 7 Deficiency; Integrin Alpha 9 Deficiency; Laminopathy; Lamin AC; SEPN 1 Related Myopathies; Bethlem Myopathy; Dystroglycanopathies; LGMD2K; LGMD2I; LGMD2L; LGMD2N; Actin Aggregation Myopathy; Cap Disease; Central Core Disease; Centronuclear Myopathy; Core Rod Myopathy; Hyaline Body Myopathy; Multiminicore Myopathy; Myotubular Myopathy; Nemaline Myopathy; Tubular Aggregate Myopathy; Zebra Body Disease Myopathy; Congenital Myopathy Other; Reducing Body Myopathy; Sarcotubular Myopathy; Spheroid Body Myopathy
- 9RecruitingLast Updated: December 19, 2011Condition(s): Retinitis Pigmentosa; Retinal Degeneration
- 10CompletedLast Updated: December 1, 2011Condition(s): Gout
- 11RecruitingLast Updated: October 24, 2011Condition(s): Maroteaux-lamy Disease; Lysosomal Storage Diseases
- 12AvailableLast Updated: June 6, 2011Condition(s): Acute Lymphoblastic Leukemia; Acute Myeloid Leukemia; Chronic Myeloid Leukemia; Myelodysplastic Syndrome; Lymphomas; Bone Marrow Failure; Hemoglobinopathy; Immune Deficiency; Osteopetrosis; Cytopenias; White Blood Cell Abnormalities; Red Blood Cell Abnormalities
- 13CompletedLast Updated: June 23, 2011Condition(s): Acute Gout Flare
- 14CompletedLast Updated: April 26, 2012Condition(s): Intercritical Gout
- 15CompletedLast Updated: December 1, 2011Condition(s): Gout
- 16RecruitingLast Updated: February 21, 2012Condition(s): Lysosomal Storage Diseases; Gaucher Disease; Sphingolipidoses
- 17Active, not recruitingLast Updated: May 5, 2011Condition(s): Familial Adenomatous Polyposis; Duodenal Neoplasms; Duodenal Polyps
- 18RecruitingLast Updated: October 21, 2011Condition(s): Lysosomal Storage Diseases; Pompe Disease
- 19RecruitingLast Updated: January 23, 2012Condition(s): Mucopolysaccharidosis Type III A; Sanfilippo Disease Type A
- 20CompletedLast Updated: March 13, 2012Condition(s): Huntington's Disease
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The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Genetic+Diseases%2C+Inborn%22
