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Recruiting
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
NCT01793168
- Conditions
- 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
- Locations
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- Sanford Health Sioux Falls, South Dakota, United States
- Online Patient Enrollment System Sydney, Australia
Recruiting
National Registry of Rare Kidney Diseases
NCT06065852
- Conditions
- AH Amyloidosis, AHL Amyloidosis, AL Amyloidosis, +207 more
- Locations
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- Zoe Plummer Bristol, South West, United Kingdom
NCT07605884
- Conditions
- Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Denys-Drash Syndrome, +21 more
- Locations
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- Hôpital Femme Mère Enfant, Hospices Civils de Lyon Bron, France
- CHU de Lille Lille, France
- CHU Montpellier Montpellier, France
- CHU de Nancy - Hôpitaux de Brabois Nancy, France
Completed
Registry for Patients With Wilms' Tumor Suppressor Gene 1 (WT1) Mutation Associated Diseases
NCT01252901
- Conditions
- Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +35 more
- Locations
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- Universitätskrankenhaus Hamburg-Eppendorf Hamburg, Germany