Cerebellar Disease,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Seckel Syndrome,Riddle Syndrome,Lig4 Syndrome,Renal Cell Carcinoma, Nonpapillary,Nijmegen Breakage Syndrome,Ataxia-Telangiectasia,Primary Autosomal Recessive Microcephaly

Breast Cancer,Gastric Cancer,Lung Squamous Cell Carcinoma,Lung Cancer

Fanconi Anemia, Complementation Group J,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Seckel Syndrome,Ataxia-Telangiectasia

Cancerophobia,Skin Melanoma,Ovarian Carcinosarcoma,Uterine Carcinosarcoma,Endometrial Cancer,Peritoneum Cancer,Endosalpingiosis,Ganglioneuroblastoma,Breast-Ovarian Cancer, Familial 2,Retinitis Pigmentosa,Adenoid Cystic Carcinoma,Cowden Syndrome,Cowden Syndrome 1,Primary Peritoneal Carcinoma,Cervical Adenoma Malignum,Fallopian Tube Disease,Fallopian Tube Carcinoma,Bilateral Breast Cancer,Synchronous Bilateral Breast Carcinoma,B-Lymphoblastic Leukemia/Lymphoma,Uterine Corpus Cancer,B-Lymphoblastic Leukemia/Lymphoma With Hyperdiploidy,Dysgerminoma,Alzheimer Disease,Familiar Ovarian Carcinoma,Basaloid Lung Carcinoma,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Hereditary Site-Specific Ovarian Cancer Syndrome,Familial Ovarian Cancer,Amelogenesis Imperfecta,Ovarian Serous Cystadenofibroma,Female Reproductive System Disease,Neuroblastoma,Inherited Cancer-Predisposing Syndrome,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Cystinuria,Thoracic Cancer,Canavan Disease,Papillary Serous Adenocarcinoma,Cystadenoma,Intracystic Papillary Adenoma,Mulchandani-Bhoj-Conlin Syndrome,Dysplastic Nevus Syndrome,Bladder Cancer,Fallopian Tube Clear Cell Adenocarcinoma,Cerebellar Disease,Endocrine System Disease,Deafness, Autosomal Dominant 13,Fanconi Anemia, Complementation Group J,Ovarian Serous Adenofibroma,Cockayne Syndrome,Tetraploidy,Aplastic Anemia,Ovarian Cancer,Adenocarcinoma,In Situ Carcinoma,Female Reproductive Endometrioid Cancer,Breast Ductal Carcinoma,Lobular Neoplasia,Breast Carcinoma In Situ,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Hypertrophy Of Breast,Endometrial Serous Adenocarcinoma,Cystadenocarcinoma,Papillary Adenocarcinoma,Serous Cystadenocarcinoma,Premature Menopause,Microcephaly,Rhabdomyosarcoma,Werner Syndrome,Ovarian Cystadenoma,Ovarian Disease,Deficiency Anemia,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Palmoplantar Keratoderma, Punctate Type Ii,Skin Carcinoma,Gastric Cancer,Fanconi Anemia, Complementation Group S,Breast Disease,Prostate Cancer,Disease Of Mental Health,Ovarian Cystadenocarcinoma,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Congenital Myasthenic Syndrome,Mutagen Sensitivity,Breast Fibroadenoma,Fallopian Tube Adenocarcinoma,Ovary Adenocarcinoma,Breast-Ovarian Cancer, Familial 1,Ruvalcaba Syndrome,Lynch Syndrome,Lung Squamous Cell Carcinoma,Ovary Transitional Cell Carcinoma,Neural Tube Defects,Fanconi Anemia, Complementation Group D1,Cockayne Syndrome B,Seckel Syndrome,Tooth Agenesis,Body Mass Index Quantitative Trait Locus 20,Riddle Syndrome,Female Breast Cancer,Gastric Cancer, Hereditary Diffuse,Pancreatic Cancer 4,Tumor Predisposition Syndrome,Autosomal Genetic Disease,Ewing Sarcoma,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Nephrolithiasis/Osteoporosis, Hypophosphatemic, 2,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Ovarian Serous Carcinoma,Autosomal Recessive Cerebellar Ataxia,Nosophobia,Pre-Malignant Neoplasm,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Estrogen-Receptor Negative Breast Cancer,Breast Benign Neoplasm,Thoracic Benign Neoplasm,Ovarian Benign Neoplasm,Nijmegen Breakage Syndrome,Li-Fraumeni Syndrome,Ovarian Cancer 1,Punctate Palmoplantar Keratoderma,Myasthenic Syndrome, Congenital, 6, Presynaptic,Ataxia-Telangiectasia,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Bloom Syndrome,Primary Autosomal Recessive Microcephaly,Lung Cancer,Pancreatic Cancer

Breast Cancer,Prostate Calculus,Kabuki Syndrome 1

Follicular Adenoma,Microcephaly Chorioretinopathy Recessive Form,Dyskeratosis Congenita,Cerebellar Disease,Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome,Primary Hyperoxaluria,Breast Cancer,Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation,Microcephaly,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Hutchinson-Gilford Progeria Syndrome,Myeloproliferative Disorder, Chronic, With Eosinophilia,Seckel Syndrome,Riddle Syndrome,Microcephaly And Chorioretinopathy, Autosomal Recessive, 3,Lig4 Syndrome,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Autosomal Recessive Cerebellar Ataxia,Ataxia-Telangiectasia,Primary Autosomal Recessive Microcephaly

Squamous Cell Carcinoma,Childhood Acute Lymphocytic Leukemia,Gastric Cardia Carcinoma,Mucositis,Gastroesophageal Adenocarcinoma,Spinocerebellar Ataxia, Autosomal Recessive 24,Oral Leukoplakia,Senile Cataract,Differentiated Thyroid Carcinoma,Spinocerebellar Ataxia Type 1 With Axonal Neuropathy,Sporadic Breast Cancer,Basal Cell Carcinoma,Leukemia, Acute Lymphoblastic,Cataract,Oculomotor Apraxia,Larynx Cancer,Bladder Cancer,Fibrosclerosis Of Breast,Cardia Cancer,Breast Cancer,Colorectal Cancer,Spinocerebellar Ataxia, Autosomal Recessive 26,Non-Proliferative Fibrocystic Change Of The Breast,Xeroderma Pigmentosum, Complementation Group A,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group G,Skin Carcinoma,Gastric Cancer,Breast Disease,Prostate Cancer,Mutagen Sensitivity,Lynch Syndrome,Sister Chromatid Exchange, Frequency Of,Esophageal Cancer,Seckel Syndrome,Female Breast Cancer,Tobacco Addiction,Lig4 Syndrome,Colorectal Adenoma,Nasopharyngeal Carcinoma,Apraxia,Ataxia-Telangiectasia,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Lung Cancer

Cowden Syndrome,Plasma Cell Neoplasm,Fallopian Tube Carcinoma,Neuroblastoma,Inherited Cancer-Predisposing Syndrome,Sporadic Breast Cancer,Ovarian Cancer,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Fanconi Anemia, Complementation Group A,Lynch Syndrome,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Li-Fraumeni Syndrome,Myeloma, Multiple

Physical Disorder,Microcephaly 17, Primary, Autosomal Recessive,Microcephaly 9, Primary, Autosomal Recessive,Microcephaly 7, Primary, Autosomal Recessive,Microcephaly 6, Primary, Autosomal Recessive,Microcephaly 5, Primary, Autosomal Recessive,Congenital Nervous System Abnormality,Microcephaly 18, Primary, Autosomal Dominant,Microcephaly,Microcephaly 11, Primary, Autosomal Recessive,Disease Of Mental Health,Seckel Syndrome 4,Microcephaly 2, Primary, Autosomal Recessive, With Or Without Cortical Malformations,Microcephaly 4, Primary, Autosomal Recessive,Seckel Syndrome 5,Microcephaly 3, Primary, Autosomal Recessive,Periventricular Nodular Heterotopia,Microcephaly 13, Primary, Autosomal Recessive,Microcephaly 12, Primary, Autosomal Recessive,Seckel Syndrome,Seckel Syndrome 2,Miller-Dieker Lissencephaly Syndrome,Microcephaly 8, Primary, Autosomal Recessive,Microcephaly 1, Primary, Autosomal Recessive,Autosomal Recessive Non-Syndromic Intellectual Disability,Ataxia-Telangiectasia,Autism,Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii,Primary Autosomal Recessive Microcephaly,Primary Microcephaly,Band Heterotopia,Isolated Growth Hormone Deficiency, Type Ia