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Nume Dysostosis
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Boli A-Z Acral Dysostosis Dyserythropoiesis Syndrome Acrocallosal Syndrome Acrocraniofacial Dysostosis Acrodysostosis Acrofacial Dysostosis Acrofacial Dysostosis 1, Nager Type Acrofacial Dysostosis, Cincinnati Type Acrofacial Dysostosis, Palagonia Type Acrofacial Dysostosis Syndrome of Rodriguez Acrofrontofacionasal Dysostosis Acrofrontofacionasal Dysostosis 1 Acromelic Frontonasal Dysostosis Aging Alopecia Al-Raqad Syndrome Aniridia 1 Ankylosis Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrioventricular Septal Defect Autosomal Dominant Disease Ayme-Gripp Syndrome Beare-Stevenson Cutis Gyrata Syndrome Biliary Atresia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Bone Development Disease Brachydactyly Branchial Arch Syndrome, X-Linked Brittle Bone Disorder Bronchomalacia Cartilage-Hair Hypoplasia Cataract Central Core Disease of Muscle Cerebritis Cerebrocostomandibular Syndrome Cervicitis Choanal Atresia, Posterior Chondrodysplasia Punctata 2, X-Linked Dominant Chromosome 2q35 Duplication Syndrome Cleft Lip Cleft Lip/palate Cleidocranial Dysplasia Cleidocranial Dysplasia, Recessive Form Cleidocranial Dysplasia Spectrum Disorder Congenital Disorder of Glycosylation, Type Ie Congenital Nystagmus Congenital Pseudoarthrosis of the Tibia Conjunctivitis Coxa Vara Cranioectodermal Dysplasia 1 Craniofacial Dyssynostosis Craniofacial Microsomia Craniofrontonasal Syndrome Craniosynostosis Craniosynostosis 1 Crouzon Syndrome Cystic Kidney Disease Dextrocardia Dextrocardia with Situs Inversus Diamond-Blackfan Anemia Diaphanospondylodysostosis Duodenitis Dwarfism Ellis-Van Creveld Syndrome Epilepsy Esophageal Atresia Exocrine Pancreatic Insufficiency Exostoses, Multiple, Type Ii Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Fanconi Anemia, Complementation Group E Femur-Fibula-Ulna Syndrome Fragile X Syndrome Frontofacionasal Dysplasia Gigantism Gorlin-Chaudhry-Moss Syndrome Hajdu-Cheney Syndrome Hemangioma Hemifacial Microsomia Hepatic Adenomas, Familial Hermansky-Pudlak Syndrome Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypertrophic Cardiomyopathy Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypomandibular Faciocranial Dysostosis Hypoparathyroidism Hypospadias Hypotonia Intracranial Hypertension Ischemia Ischio-Vertebral Syndrome Jackson-Weiss Syndrome Johnson Neuroectodermal Syndrome Kallmann Syndrome Larsen Syndrome Laryngitis Leiomyoma Limb Ischemia Lipomyelomeningocele Lymphedema Macrostomia, Isolated Mandibulofacial Dysostosis, Guion-Almeida Type Mandibulofacial Dysostosis with Alopecia Mandibulofacial Dysostosis with Macroblepharon and Macrostomia Mast Cell Activation Syndrome Maxillary Sinusitis Maxillofacial Dysostosis Maxillonasal Dysplasia, Binder Type Microcephaly Microphthalmia Microtia Mongolian Spot Mucopolysaccharidosis-Plus Syndrome Multiple Mitochondrial Dysfunctions Syndrome 5 Myelomeningocele Nephronophthisis Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurodegeneration with Brain Iron Accumulation 2a Neutropenia Oculodentodigital Dysplasia Omphalocele Orofacial Cleft Orofaciodigital Syndrome Osteoglophonic Dysplasia Osteopetrosis Palatopharyngeal Incompetence Pancreatitis Parietal Foramina Pectus Carinatum Pelvis-Shoulder Dysplasia Periodontitis Peripheral Dysostosis Phocomelia Pierre Robin Syndrome Pierre Robin Syndrome and Oligodactyly Pili Gemini Plagiocephaly Polydactyly Polydactyly, Postaxial, Type A1 Polykaryocytosis Inducer Postaxial Acrofacial Dysostosis Potocki-Shaffer Syndrome Pseudohypoparathyroidism Ptosis Pycnodysostosis Pyle Disease Radin Blood Group Antigen Restrictive Dermopathy, Lethal Reticular Dysgenesis Robin Sequence with Cleft Mandible and Limb Anomalies Saethre-Chotzen Syndrome Scoliosis Sensorineural Hearing Loss Sinusitis Situs Inversus Skeletal Dysplasias Sleep Apnea Sotos Syndrome 1 Spondylocostal Dysostosis 1, Autosomal Recessive Spondylocostal Dysostosis 3, Autosomal Recessive Spondylocostal Dysostosis 5 Spondylocostal Dysostosis, Autosomal Recessive Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Spondylospinal Thoracic Dysostosis Strabismus Swine Influenza Syringomyelia Telecanthus Tetralogy of Fallot Tetrasomy 9p Three M Syndrome 1 Thyroiditis Tibial Hemimelia Treacher Collins Syndrome 1 Urinary System Disease Ventricular Septal Defect Weyers Acrofacial Dysostosis X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome