DISEASES Musculoskeletal Diseases [C05] Musculoskeletal Diseases Bone Diseases [C05.116] Bone Diseases Cartilage Diseases [C05.182] Cartilage Diseases Fasciitis [C05.321] Fasciitis Foot Deformities [C05.330] Foot Deformities Foot Diseases [C05.360] Foot Diseases Hand Deformities [C05.390] Hand Deformities Jaw Diseases [C05.500] Jaw Diseases Joint Diseases [C05.550] Joint Diseases Muscular Diseases [C05.651] Muscular Diseases Musculoskeletal Abnormalities [C05.660] Musculoskeletal Abnormalities Arthrogryposis [C05.660.077] Arthrogryposis Campomelic Dysplasia [C05.660.142] Campomelic Dysplasia Craniofacial Abnormalities [C05.660.207] Craniofacial Abnormalities Developmental Dysplasia of the Hip [C05.660.297] Developmental Dysplasia of the Hip Funnel Chest [C05.660.386] Funnel Chest Gastroschisis [C05.660.417] Gastroschisis Klippel-Feil Syndrome [C05.660.551] Klippel-Feil Syndrome Limb Deformities, Congenital [C05.660.585] Limb Deformities, Congenital Pectus Carinatum [C05.660.745] Pectus Carinatum Synostosis [C05.660.906] Synostosis Rheumatic Diseases [C05.799] Rheumatic Diseases DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormalities [C16.131] Congenital Abnormalities Abnormalities, Drug-Induced [C16.131.042] Abnormalities, Drug-Induced Abnormalities, Multiple [C16.131.077] Abnormalities, Multiple Abnormalities, Radiation-Induced [C16.131.080] Abnormalities, Radiation-Induced Abnormalities, Severe Teratoid [C16.131.085] Abnormalities, Severe Teratoid Aicardi Syndrome [C16.131.162] Aicardi Syndrome Cardiovascular Abnormalities [C16.131.240] Cardiovascular Abnormalities Chromosome Disorders [C16.131.260] Chromosome Disorders Congenital Microtia [C16.131.287] Congenital Microtia Digestive System Abnormalities [C16.131.314] Digestive System Abnormalities Eye Abnormalities [C16.131.384] Eye Abnormalities Hernias, Diaphragmatic, Congenital [C16.131.433] Hernias, Diaphragmatic, Congenital Lymphatic Abnormalities [C16.131.482] Lymphatic Abnormalities Musculoskeletal Abnormalities [C16.131.621] Musculoskeletal Abnormalities Arthrogryposis [C16.131.621.077] Arthrogryposis Campomelic Dysplasia [C16.131.621.142] Campomelic Dysplasia Cervical Rib Syndrome [C16.131.621.174] Cervical Rib Syndrome Craniofacial Abnormalities [C16.131.621.207] Craniofacial Abnormalities Developmental Dysplasia of the Hip [C16.131.621.297] Developmental Dysplasia of the Hip Funnel Chest [C16.131.621.386] Funnel Chest Gastroschisis [C16.131.621.417] Gastroschisis Hajdu-Cheney Syndrome [C16.131.621.445] Hajdu-Cheney Syndrome Hip Dislocation, Congenital [C16.131.621.449] Hip Dislocation, Congenital Klippel-Feil Syndrome [C16.131.621.551] Klippel-Feil Syndrome Laryngomalacia [C16.131.621.568] Laryngomalacia Limb Deformities, Congenital [C16.131.621.585] Limb Deformities, Congenital Pectus Carinatum [C16.131.621.745] Pectus Carinatum Synostosis [C16.131.621.906] Synostosis Tracheobronchomalacia [C16.131.621.953] Tracheobronchomalacia Nervous System Malformations [C16.131.666] Nervous System Malformations Respiratory System Abnormalities [C16.131.740] Respiratory System Abnormalities Situs Inversus [C16.131.810] Situs Inversus Skin Abnormalities [C16.131.831] Skin Abnormalities Stomatognathic System Abnormalities [C16.131.850] Stomatognathic System Abnormalities Thyroid Dysgenesis [C16.131.894] Thyroid Dysgenesis Urogenital Abnormalities [C16.131.939] Urogenital Abnormalities

Musculoskeletal Abnormalities - Concept préféré

Concept UI	M0014258
Note d'application	Congenital structural abnormalities and deformities of the musculoskeletal system.
Terme préféré	Musculoskeletal Abnormalities
Synonymes	Abnormalities, Musculoskeletal Abnormality, Musculoskeletal Musculoskeletal Abnormality