Clinical Trials

1,250 enrolled

Diabetes Mellitus, Type 2, Pancreatic Cyst, Prediabetic State, Genetic Predisposition to Disease, Genetic Diseases, Inborn, Pancreatitis, Chronic

NCT05587439 2025-07-10

INHERIT

500 enrolled

Thoracic

Lung Neoplasms, Genetic Predisposition to Disease, Genetic Diseases, Inborn

NCT06990633 2025-05-25

LYNX

Not yet recruiting

180 enrolled

Colonic Neoplasms, Colorectal Neoplasms, Hereditary Nonpolyposis, Colorectal Neoplasms, Genetic Diseases, Inborn

NCT04880356 2024-11-19

Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.

100 enrolled

2-Hydroxyglutaricaciduria, Fahr's disease, Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, Methylmalonic acidemia with homocystinuria, Undiagnosed Diseases, Adrenoleukodystrophy, Cysts, Hepatolenticular Degeneration, Leukodystrophy, Globoid Cell, Leukodystrophy, Metachromatic, Metabolic Diseases, Nervous System Diseases, Sphingolipidoses, Xanthomatosis, Cerebrotendinous, Pelizaeus-Merzbacher Disease, Genetic Diseases, Inborn, Rare Diseases, Alexander Disease, Leukoencephalopathies

NCT04682470 2022-03-02

COMPRAYA

4,000 enrolled

Infertility, Neoplasms, Neoplasms, Second Primary, Genetic Diseases, Inborn

NCT00366509 2021-08-02

Role of Helicobacter Pylori and Its Toxins in Lung and Digestive System Diseases

157 enrolled

Asthma, Lung Diseases, Pulmonary Fibrosis, Sarcoidosis, Lymphangioleiomyomatosis, Genetic Diseases, Inborn

NCT04428710 2021-02-11

Assessment Psychological Distress for Cancer Heredity Test

Unknown

800 enrolled

Neoplasms, Genetic Diseases, Inborn

NCT02198092 2019-08-28

Septin9

24 enrolled

Colorectal Neoplasms, Hereditary Nonpolyposis, Adenomatous Polyposis Coli, Colorectal Neoplasms, Genetic Diseases, Inborn

NCT01645904 2019-05-28

A Social Media Approach to Improve Genetic Risk Communication Phase I

Unknown

49 enrolled

Colorectal Neoplasms, Hereditary Nonpolyposis, Genetic Diseases, Inborn

NCT01369953 2018-07-26

Informed Consent for Whole Genome Sequencing: Ideals and Norms Referenced by Early Participants

30 enrolled

Head & Neck

Hyperparathyroidism 2, Coronary Artery Disease, Proteus Syndrome, Genetic Diseases, Inborn

NCT00068146 2018-07-05

Fluorodeoxyglucose-Positron Emission Tomography (FDG-PET) to Evaluate Autoimmune Lymphoproliferative Syndrome (ALPS) and ALPS-associated Lymphoma

77 enrolled

Lymphoid

Lymphadenopathy, Lymphoma, Lymphoproliferative Disorders, Syndrome, Genetic Diseases, Inborn

NCT00005900 2005-06-24

Study of Pulmonary Complications in Pediatric Patients With Storage Disorders Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Unknown

10 enrolled

Adrenoleukodystrophy, Fucosidosis, Gaucher Disease, Leukodystrophy, Globoid Cell, Leukodystrophy, Metachromatic, Mucopolysaccharidosis I, Metabolism, Inborn Errors, Mucolipidoses, Mucopolysaccharidoses, Mucopolysaccharidosis VI, Niemann-Pick Diseases, Sphingolipidoses, Wolman Disease, Genetic Diseases, Inborn, Rare Diseases, Mannosidase Deficiency Diseases

NCT00007046 2005-06-24

Genetic Study of Patients and Families With Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma of the Bone