Phenotype, Genotype and Biomarkers 2 | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Phenotype, Genotype and Biomarkers 2	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Frontotemporal Lobar Degeneration, Nutritional and Metabolic Diseases, TDP-43 proteinopathy, amyotrophic lateral sclerosis, brain disorder, central nervous system disorder, central nervous system malformation, cognitive disorder, dementia, frontotemporal dementia, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, inherited neurodegenerative disorder, lateral sclerosis, metabolic disease, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, progressive muscular atrophy, proteostasis deficiencies, psychiatric disorder, spinal cord disorder, spinal muscular atrophy	Active, not recruiting	Not stated	2026-06-15		NCT04875416

3 results · Page 1 of 1

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Organizations	Linked trials
National Institute of Neurological Disorders and Stroke (NINDS)	370
National Institutes of Health (NIH)	667
University of Miami	277

4 results · Page 1 of 1

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Research sites	City	Country	Linked trials
University of Cape Town	Cape Town	South Africa	10
University of Kansas Medical Center	Kansas City	United States	240
University of Miami	Miami	United States	327
University of Pennsylvania	Philadelphia	United States	507