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Chronic disease of musculoskeletal system 128237006 SNOMED CT code SNOMED code 128237006 name Chronic disease of musculoskeletal system status active date introduced 2002-01-31 fully specified name(s) Chronic disease of musculoskeletal system (disorder) synonyms Chronic musculoskeletal disorder Chronic musculoskeletal disease Chronic disease of the musculoskeletal system Chronic disease of musculoskeletal system attributes - group1 Clinical course Chronic 90734009 attributes - group2 Finding site Musculoskeletal structure 26107004 parents children Adynamic bone disease 236552002 Allan-Herndon-Dudley syndrome 702327009 Alpha-B crystallin-related late-onset myopathy 783770002 Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis 829973009 Autosomal dominant mitochondrial myopathy with exercise intolerance 1222644009 Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy 1222704008 Autosomal recessive lower motor neuron disease with childhood onset 771302009 Benign monomelic amyotrophy 230256009 Childhood-onset nemaline myopathy 1197154006 Childhood-onset spasticity with hyperglycinemia 773492007 Chronic abscess of jaw 73345000 Chronic alcoholic myopathy 838376007 Chronic arthropathy 38850007 Chronic bursitis 109299008 Chronic hiccup 716771000 Chronic kidney disease with osteoporosis 897308007 removed: 2023-12-01 Chronic mastoiditis 80645004 Chronic musculoskeletal pain due to disease of nervous system 762598004 Chronic musculoskeletal pain due to persistent inflammation 762597009 Chronic osteitis of jaw 196461003 Chronic osteomyelitis 40970001 Chronic perichondritis of pinna 45431004 Chronic petrositis 28593007 Chronic rupture of Achilles tendon 700377000 Diaphyseal dysplasia 34643004 Early-onset calcifying leukoencephalopathy, skeletal dysplasia 1222661007 Elastotic nodules of antihelix 72898003 Epiphyseal dysplasia 254080004 Familial gigantiform cementoma of jaw 1263445009 Fibromyositis 24693007 Hand-Schüller-Christian disease 39795003 Hemifacial spasm 13753008 Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome 771306007 Huntington's chorea 58756001 Intermediate nemaline myopathy 1197156008 Intermittent torticollis 202767003 Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome 1172590009 Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome 1172591008 Langer mesomelic dysplasia syndrome 38494008 Majeed syndrome 703540008 Muscular dystrophy 73297009 Myoclonic epilepsy with ragged red fibers 230426003 Myofascial pain syndrome 726531007 NARP syndrome 237984008 Necrosis of ankle muscle co-occurrent and due to chronic ulcer of ankle 10637871000119103 Necrosis of lower leg muscle co-occurrent and due to chronic ulcer of lower leg 10641511000119103 Necrosis of muscle of buttock co-occurrent and due to chronic ulcer of buttock 10642151000119103 Necrosis of sacral muscle co-occurrent and due to chronic ulcer of sacrum 10642311000119101 Night blindness, skeletal anomalies, dysmorphism syndrome 1237228009 Non-traumatic acute-on-chronic slipped upper femoral epiphysis 203375003 Non-traumatic chronic slipped upper femoral epiphysis 203376002 Osteonecrosis of ankle bone due to chronic ulcer of ankle 10637791000119107 Osteonecrosis of fibula due to chronic ulcer of calf 10640831000119104 Osteonecrosis of sacral bone due to chronic ulcer of sacrum 10642191000119108 Osteopetrosis 1926006 Osteoporosis due to chronic kidney disease 1295482007 Osteosclerosis 49347007 Paroxysmal rhabdomyolysis 1148631003 Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome 782752005 Persistent congenital anteversion of femur 1236806006 Persistent neonatal myasthenia gravis 193206003 Polyglucosan body myopathy type 2 1228849007 Primary fibromyalgia syndrome 95417003 Progressive avascular necrosis of lunate 787484007 Progressive external ophthalmoplegia 46252003 Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome 1187303004 Proximal myopathy with focal depletion of mitochondria 1197756002 Renal osteodystrophy 16726004 Renal osteodystrophy with high bone turnover 897310009 Renal osteodystrophy with low bone turnover 897312001 Renal osteodystrophy with normal bone turnover 897311008 Severe oculo-renal-cerebellar syndrome 1208341008 Spastic paraplegia with Paget disease of bone syndrome 726622002 Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome 719205008 Tendinosis 724152009 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 27624003 128237006 138875005 404684003 106028002 928000 128237006 ancestors sorted most to least specific
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