Page 1 of Clinical Trials for genetic diseases and dysmorphic syndromes, 68 Total Matches

Condition(s): X-Linked Agammaglobulinemia; X-Linked Hyper IgM Syndrome; Wiskott-Aldrich Syndrome; Leukocyte Adhesion Deficiency Syndrome

Condition(s): Immunologic Deficiency Syndromes; Chediak-Higashi Syndrome; Common Variable Immunodeficiency; Graft Versus Host Disease; X-Linked Lymphoproliferative Syndrome; Familial Erythrophagocytic Lymphohistiocytosis; Hemophagocytic Lymphohistiocytosis; X-linked Agammaglobulinemia; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; X-linked Hyper IgM Syndrome; Severe Combined Immunodeficiency; Leukocyte Adhesion Deficiency Syndrome; Virus-Associated Hemophagocytic Syndrome

Condition(s): Thrombocytopenia; Metachromatic Leukodystrophy; Fanconi's Anemia; Thalassemia Major; Pure Red-Cell Aplasia; Inborn Errors of Metabolism

Condition(s): Primary Ciliary Dyskinesia

Condition(s): Williams Syndrome; Angelman Syndrome; Prader-Willi Syndrome; Shprintzen Syndrome; Smith-Magenis Syndrome; DiGeorge Syndrome; Chromosome Abnormalities

Condition(s): Turner's Syndrome

Condition(s): Turner's Syndrome

Condition(s): Werner's Syndrome

Condition(s): Stenosis; Histiocytoma

Condition(s): Chediak-Higashi Syndrome; Graft Versus Host Disease; X-Linked Lymphoproliferative Syndrome; Familial Erythrophagocytic Lymphohistiocytosis; Hemophagocytic Lymphohistiocytosis; Virus-Associated Hemophagocytic Syndrome

Condition(s): Epidermolysis Bullosa

Condition(s): Ornithine Transcarbamylase Deficiency Disease

Condition(s): Alpha 1-Antitrypsin Deficiency

Condition(s): Neurofibromatosis 2

Condition(s): Cystic Fibrosis

Condition(s): Cystic Fibrosis

Condition(s): Cystic Fibrosis