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Boli A-Z Acanthoma Achondroplasia Acrocallosal Syndrome Adie Pupil Agammaglobulinemia Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Ankylosis Anorectal Anomalies Anorexia Nervosa 1 Antley-Bixler Syndrome Apert Syndrome Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Auriculocondylar Syndrome 1 B Cell Deficiency Beare-Stevenson Cutis Gyrata Syndrome Blood Group--Ahonen Blood Group, I System Bone Development Disease Brachydactyly Brachydactyly, Type D Brittle Bone Disorder Burkitt Lymphoma Clear Cell Acanthoma Cockayne Syndrome Collagen Disease Common Variable Immunodeficiency Congenital Tracheal Stenosis Craniosynostosis Crouzon Syndrome Deafness, Autosomal Recessive 51 Ehlers-Danlos Syndrome, Classic Type, 1 Fanconi Anemia, Complementation Group E Fgfr-Related Craniosynostosis Syndromes Hartsfield Syndrome Hepatic Adenomas, Familial Hydrocephalus Hypochondroplasia Hypospadias Isolated Brachycephaly Isolated Plagiocephaly Jackson-Weiss Syndrome Juvenile Hereditary Hemochromatosis Lacrimoauriculodentodigital Syndrome Larsen-Like Syndrome Laryngomalacia Lung Lymphoma Luteoma Mature B-Cell Neoplasm Muenke Syndrome Osteochondrodysplasia Osteogenesis Imperfecta, Type Ii Osteoglophonic Dysplasia Papilledema Plagiocephaly Proteus Syndrome Radioulnar Synostosis Robinow Syndrome Saethre-Chotzen Syndrome Spondylocostal Dysostosis 1, Autosomal Recessive Spondyloepiphyseal Dysplasia Congenita Synostosis Synovial Chondromatosis Thanatophoric Dysplasia, Type I Tracheal Stenosis Vasomotor Rhinitis Vulvitis