Ignite Creation Date:
2024-05-05 @ 10:22 AM
Last Modification Date:
2024-10-26 @ 9:04 AM
Study NCT ID:
NCT00004341
Status:
UNKNOWN
Last Update Posted:
2005-06-24
First Post:
1999-10-18
Brief Title:
Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders
Sponsor:
Eunice Kennedy Shriver National Institute of Child Health and Human Development NICHD
Organization:
Office of Rare Diseases ORD
Conditions & Keywords Data
Conditions:
| Name |
|---|
| Leukocyte Adhesion Deficiency Syndrome |
| X-Linked Agammaglobulinemia |
| X-Linked Hyper IgM Syndrome |
| Wiskott-Aldrich Syndrome |
Keywords:
| Name | View |
|---|---|
| rare disease | View |
| Wiskott-Aldrich syndrome | View |
| X-linked agammaglobulinemia | View |
| X-linked hyper IgM syndrome | View |
| genetic diseases and dysmorphic syndromes | View |
| immunologic disorders and infectious disorders | View |
| leukocyte adhesion deficiency syndrome | View |
| primary immunodeficiency disease | View |