Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders - Related Studies

Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders

This study is ongoing, but not recruiting participants.

Study NCT00004341. Last updated on June 23, 2005. Information provided by Office of Rare Diseases (ORD)

Find Related Studies by Searching for the Conditions, Interventions, and Sponsors found in this study:


1	Conditions listed in this trial
		X-Linked Agammaglobulinemia
		X-Linked Hyper IgM Syndrome
		Wiskott-Aldrich Syndrome

2	Additional conditions recognized in this trial
		Adhesions
		Agammaglobulinemia
		Hyper-IgM Immunodeficiency Syndrome
		Hyper-IgM Immunodeficiency Syndrome, Type 1
		Leukocyte-Adhesion Deficiency Syndrome
		Syndrome

3	More general conditions related to this trial
		Blood Coagulation Disorders
		Blood Coagulation Disorders, Inherited
		Blood Platelet Disorders
		Blood Protein Disorders
		Disease
		Dysgammaglobulinemia
		Genetic Diseases, Inborn
		Genetic Diseases, X-Linked
		Hematologic Diseases
		Hemorrhagic Disorders
		Immune System Diseases
		Immunologic Deficiency Syndromes
		Lymphatic Diseases
		Lymphoproliferative Disorders
		Pathologic Processes
		Purpura, Thrombocytopenic
		Thrombocytopenia

4	Sponsors listed in this trial
		Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
		University of Washington