Informaţii despre

Nume Skeletal Dysplasias
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Other specified osteochondrodysplasias
Clasificare anatomică Malacards Boli osoase

Vezi şi

Boli A-Z Acanthosis Nigricans Achondrogenesis Achondrogenesis, Type Ia Achondrogenesis, Type Ib Achondrogenesis, Type Ii Achondroplasia Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans Acrocapitofemoral Dysplasia Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Amelogenesis Imperfecta Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Asphyxiating Thoracic Dystrophy Astley-Kendall Syndrome Atelosteogenesis Atelosteogenesis, Type Iii Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blount's Disease Body Mass Index Quantitative Trait Locus 1 Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Development Disease Boomerang Dysplasia Brachydactyly Brachyolmia Brittle Bone Disorder Campomelic Dysplasia Camptodactyly with Muscular Hypoplasia, Skeletal Dysplasia, and Abnormal Palmar Creases Camurati-Engelmann Disease Cartilage Disease Cerebritis Cervicitis Chondroblastoma Chondrodysplasia, Blomstrand Type Chondrodysplasia Punctata Syndrome Chondromyxoid Fibroma Chromosomal Triplication Cleft Lip Cleft Palate, Isolated Cockayne Syndrome Congenital Disorder of Glycosylation, Type Ia Congenital Subglottic Stenosis Coxa Vara Craniosynostosis Crouzon Syndrome Crouzon Syndrome with Acanthosis Nigricans Cutis Laxa Dentinogenesis Imperfecta Desbuquois Dysplasia Diastrophic Dysplasia Dwarfism Dysosteosclerosis Dysostosis Dysspondyloenchondromatosis Epilepsy Epilepsy, Familial Temporal Lobe, 1 Even-Plus Syndrome Exostoses, Multiple, Type I Familial Avascular Necrosis of the Femoral Head Frank-Ter Haar Syndrome Galactose Epimerase Deficiency Gastroduodenitis Gigantism Glucocorticoid Deficiency 3 Gonadal Dysgenesis Greenberg Dysplasia Growth Hormone Deficiency Gurrieri Syndrome Hereditary Multiple Osteochondromas Hydronephrosis Hypercalcemia, Infantile, 1 Hypercementosis Hyperparathyroidism Hypochondrogenesis Hypochondroplasia Hypopituitarism Hypotonia Hypotrichosis 8 Immunoglobulin E Concentration, Serum Inguinal Hernia Isolated Growth Hormone Deficiency, Type Ia Juxtacortical Chondroma Kashin-Beck Disease Kniest Dysplasia Kyphomelic Dysplasia Larsen Syndrome Loeys-Dietz Syndrome 3 Marshall Syndrome Meningococcemia Metaphyseal Chondrodysplasia, Jansen Type Metatropic Dysplasia Mohr Syndrome Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Multicentric Carpotarsal Osteolysis Syndrome Multifocal Osteogenic Sarcoma Multiple Epiphyseal Dysplasia Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects Muscular Dystrophy Myopathy Nephronophthisis Neuraminidase Deficiency Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuropathy Osteoarthritis Osteochondritis Dissecans Osteochondrodysplasia Osteogenic Sarcoma Osteosclerotic Metaphyseal Dysplasia Otospondylomegaepiphyseal Dysplasia Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive Pacman Dysplasia Paraphimosis Patterson Pseudoleprechaunism Syndrome Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis Platyspondylic Lethal Skeletal Dysplasia, Torrance Type Polydactyly Protein-Losing Enteropathy Pseudoachondroplasia Pseudodiastrophic Dysplasia Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ib Pycnodysostosis Pyle Disease Retinitis Retinitis Pigmentosa Rhyns Syndrome Roberts Syndrome Sarcoma Schinzel Giedion Syndrome Severe Combined Immunodeficiency Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly Skeletal Dysplasia, San Diego Type Spinal Stenosis Spondyloepimetaphyseal Dysplasia, Aggrecan Type Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Spondyloepiphyseal Dysplasia Congenita Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Spondyloperipheral Dysplasia Stickler Syndrome Stuve-Wiedemann Syndrome Synovial Chondromatosis Thanatophoric Dysplasia, Type I Thanatophoric Dysplasia, Type Ii Three M Syndrome 1 Thyroiditis Tooth Ankylosis Tooth Resorption Verloes Bourguignon Syndrome Vitreoretinal Degeneration Weismann-Netter Syndrome