Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Werner Syndrome,Fanconi Anemia, Complementation Group A,Bloom Syndrome,Rapadilino Syndrome

Anterior Horn Cell Disease,Lethal Congenital Contracture Syndrome 1,Lethal Congenital Contracture Syndrome

Seizure Disorder,Neuromuscular Disease,Corpus Callosum, Agenesis Of,Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Neuromuscular Oculoauditory Syndrome,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome

X-Linked Nephrolithiasis Type I,Robinow Syndrome, Autosomal Dominant 1,Robinow Syndrome

Retinitis Pigmentosa,Burn-Mckeown Syndrome,Distal Hereditary Motor Neuronopathy Type 2,Cockayne Syndrome,Spinal Muscular Atrophy, Type I

Metaphyseal Chondrodysplasia, Schmid Type,Robin Sequence With Cleft Mandible And Limb Anomalies,Dysostosis,Vaginal Cancer,Neurodegeneration With Brain Iron Accumulation,Thrombocytopenia-Absent Radius Syndrome,Mandibulofacial Dysostosis, Guion-Almeida Type,Acrofacial Dysostosis

Ovary Sarcoma

Hepatitis C,Hepatitis B,Venezuelan Equine Encephalitis,Encephalitis,Corpus Callosum, Agenesis Of, With Facial Anomalies And Robin Sequence,Lymphocytic Choriomeningitis,Rare Genetic Intellectual Disability,Hepatitis,Infratentorial Cancer,Ddx3x-Related Neurodevelopmental Disorder,Basal Cell Nevus Syndrome,Precursor T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Microcephaly,Hepatitis C Virus,Alacrima, Achalasia, And Mental Retardation Syndrome,Noonan Syndrome 3,Disease Of Mental Health,Adult Medulloblastoma,Childhood Medulloblastoma,Intellectual Developmental Disorder, X-Linked, Syndromic, Snijders Blok Type,Ewing Sarcoma,Syndromic Intellectual Disability,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Medulloblastoma,Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma Of Childhood,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay

Nodal Marginal Zone Lymphoma,Non-Specific Syndromic Intellectual Disability,Noonan Syndrome 3,Telecanthus,Intellectual Developmental Disorder With Impaired Language And Dysmorphic Facies

Neuropathy, Hereditary Motor And Sensory, Russe Type,Leigh Syndrome

Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Familial Colorectal Cancer,Inherited Cancer-Predisposing Syndrome,Wilms Tumor Predisposition,Ovarian Cancer,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Microcephaly,Werner Syndrome,Fanconi Anemia, Complementation Group A,Cone-Rod Dystrophy 2,Tumor Predisposition Syndrome,Syndromic Intellectual Disability,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Nijmegen Breakage Syndrome,Ataxia-Telangiectasia,Bloom Syndrome,Rapadilino Syndrome

Retinitis Pigmentosa 19,Poikiloderma With Neutropenia

Bone Development Disease,Saethre-Chotzen Syndrome,Malignant Fibrous Histiocytoma,Plasma Cell Neoplasm,Uterine Adnexa Cancer,Rothmund-Thomson Syndrome, Type 2,Synostosis,B-Lymphoblastic Leukemia/Lymphoma With Etv6-Runx1,Familial Retinoblastoma,Neutropenia,Radioulnar Synostosis,Baller-Gerold Syndrome,Craniosynostosis,Telangiectasis,B-Lymphoblastic Leukemia/Lymphoma With T,Cataract,Combined Immunodeficiency,Dyskeratosis Congenita,Skin Atrophy,Werner Syndrome,Lens Disease,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Pediatric Osteosarcoma,Juxtacortical Osteosarcoma,Bone Osteosarcoma,Poikiloderma With Neutropenia,Rothmund-Thomson Syndrome, Type 1,Pharynx Squamous Cell Carcinoma,Parietal Foramina,Li-Fraumeni Syndrome,Myeloma, Multiple,Bloom Syndrome,Osteogenic Sarcoma,Rapadilino Syndrome

Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Inherited Cancer-Predisposing Syndrome,Ovarian Cancer,Hereditary Breast Ovarian Cancer Syndrome,Werner Syndrome,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Bloom Syndrome,Rapadilino Syndrome