Retinitis Pigmentosa 19,Poikiloderma With Neutropenia

Interdigitating Dendritic Cell Sarcoma,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A

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

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

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

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

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

Ovary Sarcoma

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

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

Retinitis Pigmentosa,Corneal Dystrophy, Band-Shaped,Night Blindness,Fundus Dystrophy,Coloboma Of Macula,Cone-Rod Dystrophy 2,Retinitis Pigmentosa 84,Bietti Crystalline Corneoretinal Dystrophy