Skin Melanoma,Richter'S Syndrome,Retinitis Pigmentosa,Cll/Sll,Adenoid Cystic Carcinoma,Seizure Disorder,Cowden Syndrome,Plasma Cell Neoplasm,Rothmund-Thomson Syndrome, Type 2,Cervical Adenoma Malignum,Breast Juvenile Papillomatosis,Bilateral Breast Cancer,Synchronous Bilateral Breast Carcinoma,B-Cell Non-Hodgkin Lymphoma,Diffuse Gastric Cancer,B-Cell Lymphoma,Retinal Cancer,Spinocerebellar Ataxia Type 1 With Axonal Neuropathy,Endocrine Exophthalmos,Leukemia,Maxillary Sinus Adenocarcinoma,Inherited Cancer-Predisposing Syndrome,Glioma,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Telangiectasis,Hematologic Cancer,Combined Immunodeficiency,Oculomotor Apraxia,Dysplastic Nevus Syndrome,Dyskeratosis Congenita,Urethra Clear Cell Adenocarcinoma,Cerebellar Disease,Bile Duct Cystadenoma,Dystonia,T-Cell Prolymphocytic Leukemia,Prolymphocytic Leukemia,Ovarian Cancer,Burkitt Lymphoma,Testicular Cancer,T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Glioblastoma,Hereditary Breast Ovarian Cancer Syndrome,High Grade Glioma,Gliosarcoma,Giant Cell Glioblastoma,Mediastinum Liposarcoma,Colorectal Cancer,Acute Anterolateral Myocardial Infarction,Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation,Proctitis,Premature Menopause,Microcephaly,Rhabdomyosarcoma,Werner Syndrome,Xeroderma Pigmentosum, Complementation Group A,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Skin Carcinoma,Hutchinson-Gilford Progeria Syndrome,Prostate Cancer,Disease Of Mental Health,Aceruloplasminemia,Lynch Syndrome,Chromosome 13q14 Deletion Syndrome,Lymphoma, Non-Hodgkin, Familial,Renal Cell Carcinoma, Papillary, 1,Esophageal Cancer,Seckel Syndrome,Asphyxiating Thoracic Dystrophy,Immune Deficiency Disease,Myelodysplastic Syndrome,Female Breast Cancer,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Autosomal Recessive Disease,Autosomal Genetic Disease,Mantle Cell Lymphoma,Lig4 Syndrome,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Nephrolithiasis/Osteoporosis, Hypophosphatemic, 2,Cervical Dystonia,Colorectal Adenocarcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Lymphoma,Cataract 38,Apraxia,Nijmegen Breakage Syndrome,Leukemia, Chronic Lymphocytic,Li-Fraumeni Syndrome,Ataxia-Telangiectasia,Myeloma, Multiple,Medulloblastoma,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Melanoma, Cutaneous Malignant 1,Bloom Syndrome,Primary Autosomal Recessive Microcephaly,Lung Cancer,Ocular Motor Apraxia,Pancreatic Cancer

Lattice Corneal Dystrophy,Chronic Active Epstein-Barr Virus Infection,Lung Large Cell Carcinoma,Cerebellar Disease,Fanconi Anemia, Complementation Group I,Blepharophimosis,Ovarian Cancer,Breast Cancer,Microcephaly,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Seckel Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Autosomal Recessive Cerebellar Ataxia,Nijmegen Breakage Syndrome,Leukemia, Chronic Lymphocytic,Ceroid Lipofuscinosis, Neuronal, 2,Epithelial-Stromal Tgfbi Dystrophy,Ataxia-Telangiectasia,Seckel Syndrome 1,Isolated Growth Hormone Deficiency, Type Ia

Severe Combined Immunodeficiency,Melanoma,Immunodeficiency 26,Combined Immunodeficiency,Hemangioma Of Subcutaneous Tissue,Cerebellar Disease,Thymus Lymphoma,Dubowitz Syndrome,Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation,Microcephaly,Werner Syndrome,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Omenn Syndrome,Hutchinson-Gilford Progeria Syndrome,Alpha-Thalassemia,Immunodeficiency 26 With Or Without Neurologic Abnormalities,Seckel Syndrome,Alpha-Thalassemia/Mental Retardation Syndrome, X-Linked,Lig4 Syndrome,Autosomal Recessive Cerebellar Ataxia,Ataxia-Telangiectasia