Ignite Creation Date:
2024-05-05 @ 11:20 AM
Last Modification Date:
2024-10-26 @ 9:04 AM
Study NCT ID:
NCT00004378
Status:
COMPLETED
Last Update Posted:
2005-06-24
First Post:
1999-10-18
Brief Title:
Stem Cell Transplantation SCT for Genetic Diseases
Sponsor:
National Center for Research Resources NCRR
Organization:
National Center for Research Resources NCRR
Conditions & Keywords Data
Conditions:
| Name |
|---|
| Inborn Errors of Metabolism |
| Thrombocytopenia |
| Metachromatic Leukodystrophy |
| Fanconis Anemia |
| Thalassemia Major |
| Pure Red-Cell Aplasia |
Keywords:
| Name | View |
|---|---|
| thalassemia major | View |
| Fanconis anemia | View |
| amegakaryocytic thrombocytopenia | View |
| aplastic anemia | View |
| congenital pure red cell aplasia | View |
| genetic diseases and dysmorphic syndromes | View |
| hematologic disorders | View |
| inborn errors of metabolism | View |
| metachromatic leukodystrophy | View |
| pure red cell aplasia | View |
| rare disease | View |
| sphingolipidoses | View |