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4A43.21 Secondary Sjögren syndrome International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01 Secondary Sjögren syndrome is a progressive inflammatory autoimmune disease affecting the exocrine glands in the presence of other systemic autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. Lymphocytic infiltrates replace functional epithelium, leading to oral and ocular dryness.
postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed [select] MG30.30 Chronic secondary musculoskeletal pain from persistent inflammation Has causing condition - a selection is required - multiple selections are allowed [select] 4A00 Primary immunodeficiencies due to disorders of innate immunity – 4A00.0 Functional neutrophil defects – 4A00.1 Defects in the complement system – 4A00.2 Genetic susceptibility to particular pathogens – 4A00.3 Immunodeficiency with natural-killer cell deficiency – 4A00.Y Other specified primary immunodeficiencies due to disorders of innate immunity – 4A00.Z Primary immunodeficiencies due to disorders of innate immunity, unspecified –– 4A00.00 Neutrophil immunodeficiency syndrome –– 4A00.0Y Other specified functional neutrophil defects –– 4A00.0Z Functional neutrophil defects, unspecified –– 4A00.10 Immunodeficiency with an early component of complement deficiency –– 4A00.11 Immunodeficiency with a late component of complement deficiency –– 4A00.12 Immunodeficiency with factor B deficiency –– 4A00.13 Immunodeficiency with factor D anomaly –– 4A00.14 Hereditary angioedema –– 4A00.15 Acquired angioedema –– 4A00.1Y Other specified defects in the complement system –– 4A00.1Z Defects in the complement system, unspecified 4A01 Primary immunodeficiencies due to disorders of adaptive immunity – 4A01.0 Immunodeficiencies with predominantly antibody defects – 4A01.1 Combined immunodeficiencies – 4A01.2 Diseases of immune dysregulation – 4A01.3 Other well-defined immunodeficiency syndromes due to defects in adaptive immunity – 4A01.Z Primary immunodeficiencies due to disorders of adaptive immunity, unspecified –– 4A01.00 Hereditary agammaglobulinaemia with profoundly reduced or absent B cells –– 4A01.01 Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells –– 4A01.02 Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells –– 4A01.03 Transient hypogammaglobulinaemia of infancy –– 4A01.04 Immunodeficiencies with isotype or light chain deficiencies with normal number of B cells –– 4A01.05 Immunodeficiencies with severe reduction in serum IgG or IgA with normal or elevated IgM and normal numbers of B-cells –– 4A01.0Y Other specified immunodeficiencies with predominantly antibody defects –– 4A01.0Z Immunodeficiencies with predominantly antibody defects, unspecified –– 4A01.10 Severe combined immunodeficiencies –– 4A01.11 Major histocompatibility complex class I deficiency –– 4A01.12 Major histocompatibility complex class II deficiency –– 4A01.1Y Other specified combined immunodeficiencies –– 4A01.1Z Combined immunodeficiencies, unspecified –– 4A01.20 Immune dysregulation syndromes with hypopigmentation –– 4A01.21 Immune dysregulation syndromes presenting primarily with autoimmunity –– 4A01.22 Immune dysregulation syndromes presenting primarily with lymphoproliferation –– 4A01.23 Primary haemophagocytic lymphohistiocytosis –– 4A01.2Y Other specified diseases of immune dysregulation –– 4A01.2Z Diseases of immune dysregulation, unspecified –– 4A01.30 Immunodeficiency due to defects of the thymus –– 4A01.31 DNA repair defects other than combined T-cell or B-cell immunodeficiencies –– 4A01.32 Immuno-osseous dysplasia –– 4A01.33 Hepatic veno-occlusive disease - immunodeficiency syndrome –– 4A01.34 Hyperimmunoglobulin E syndromes 4A0Y Other specified primary immunodeficiencies 4A0Z Primary immunodeficiencies, unspecified 4A20 Acquired immunodeficiencies 4A20.0 Adult-onset immunodeficiency 4A20.1 Acquired immunodeficiency due to loss of immunoglobulin 4A20.Y Other specified acquired immunodeficiencies 4A20.Z Acquired immunodeficiencies, unspecified – 4A40.0 Systemic lupus erythematosus –– 4A40.00 Systemic lupus erythematosus with skin involvement –– 4A40.0Y Other specified systemic lupus erythematosus –– 4A40.0Z Systemic lupus erythematosus, unspecified 4A42 Systemic sclerosis – 4A42.0 Paediatric onset systemic sclerosis – 4A42.1 Diffuse systemic sclerosis – 4A42.2 Limited systemic sclerosis – 4A42.Z Systemic sclerosis, unspecified 4A60 Monogenic autoinflammatory syndromes – 4A60.0 Familial Mediterranean fever – 4A60.1 Cryopyrin-associated periodic syndromes – 4A60.2 Tumour necrosis factor receptor 1 associated periodic syndrome – 4A60.Y Other specified monogenic autoinflammatory syndromes – 4A60.Z Autoimflammatory syndrome, unspecified 4A61 SAPHO syndrome 4A62 Behçet disease 4A6Y Other specified autoinflammatory disorders 4A6Z Autoinflammatory disorders, unspecified 4A80 Allergic or hypersensitivity disorders involving the respiratory tract – 4A80.0 Drug-induced bronchospasm – 4A80.1 Bronchospasm provoked by allergy to food substance – 4A80.Y Other specified allergic or hypersensitivity disorders involving the respiratory tract – 4A80.Z Allergic or hypersensitivity disorders involving the respiratory tract, unspecified 4A81 Allergic or hypersensitivity disorders involving the eye 4A82 Allergic or hypersensitivity disorders involving skin or mucous membranes 4A83 Allergic or hypersensitivity disorders involving the gastrointestinal tract – 4A83.0 Food-induced eosinophilic gastroenteritis – 4A83.1 Food-induced eosinophilic oesophagitis – 4A83.Y Other specified allergic or hypersensitivity disorders involving the gastrointestinal tract – 4A83.Z Allergic or hypersensitivity disorders involving the gastrointestinal tract, unspecified 4A84 Anaphylaxis – 4A84.0 Anaphylaxis due to allergic reaction to food – 4A84.1 Drug-induced anaphylaxis – 4A84.2 Anaphylaxis due to insect venom – 4A84.3 Anaphylaxis provoked by physical factors – 4A84.4 Anaphylaxis due to inhaled allergens – 4A84.5 Anaphylaxis due to contact with allergens – 4A84.6 Anaphylaxis secondary to mast cell disorder – 4A84.Y Other specified anaphylaxis – 4A84.Z Anaphylaxis, unspecified –– 4A84.30 Exercise-induced anaphylaxis –– 4A84.31 Cold-induced anaphylaxis –– 4A84.3Y Anaphylaxis provoked by other specified physical factors –– 4A84.3Z Anaphylaxis provoked by unspecified physical factors 4A85 Complex allergic or hypersensitivity conditions – 4A85.0 Drug or pharmacological agents hypersensitivity – 4A85.1 Hypersensitivity to herbal and alternative medical therapies – 4A85.2 Food hypersensitivity – 4A85.3 Allergic or hypersensitivity reactions to arthropods – 4A85.Y Other specified complex allergic or hypersensitivity conditions – 4A85.Z Complex allergic or hypersensitivity conditions, unspecified –– 4A85.00 Drug-induced liver hypersensitivity disease –– 4A85.01 Drug-induced kidney hypersensitivity –– 4A85.02 Drug-induced cytopenia –– 4A85.03 Drug-induced vasculitis –– 4A85.04 Multiple drug hypersensitivity syndrome –– 4A85.0Y Drug hypersensitivity of other specified type –– 4A85.0Z Drug hypersensitivity of unspecified type –– 4A85.20 Food-induced gastrointestinal hypersensitivity –– 4A85.21 Food-induced urticaria or angioedema –– 4A85.22 Allergic contact dermatitis due to food allergen –– 4A85.2Y Other specified food hypersensitivity –– 4A85.2Z Food hypersensitivity, unspecified –– 4A85.30 Systemic allergic reaction due to Hymenoptera venom –– 4A85.31 Cutaneous allergic or hypersensitivity reactions to Hymenoptera venom –– 4A85.32 Cutaneous allergic or hypersensitivity reactions to arthropods 4A8Y Allergic or hypersensitivity conditions of other specified type 4A8Z Allergic or hypersensitivity conditions of unspecified type 4B00 Disorders of neutrophil number – 4B00.0 Neutropaenia – 4B00.1 Neutrophilia – 4B00.Y Other specified disorders of neutrophil number –– 4B00.00 Constitutional neutropaenia –– 4B00.01 Acquired neutropaenia –– 4B00.0Z Neutropaenia, unspecified –– 4B00.10 Constitutional neutrophilia –– 4B00.11 Acquired neutrophilia –– 4B00.1Z Neutrophilia, unspecified 4B01 Disorders of neutrophil function – 4B01.0 Constitutional disorders of neutrophil function – 4B01.1 Acquired disorders of neutrophil function – 4B01.Z Disorders of neutrophil function, unspecified –– 4B01.00 Disorders of neutrophil adhesion –– 4B01.01 Disorders of neutrophil chemotaxis –– 4B01.02 Disorders of neutrophil granule formation or release –– 4B01.03 Disorders of neutrophil oxidative metabolism –– 4B01.0Y Other specified constitutional disorders of neutrophil function –– 4B01.0Z Constitutional disorders of neutrophil function, unspecified 4B02 Eosinopenia – 4B02.0 Constitutional decrease in eosinophil number – 4B02.1 Acquired decrease in eosinophil number – 4B02.Z Eosinopenia, unspecified 4B03 Eosinophilia – 4B03.0 Constitutional eosinophilia – 4B03.1 Acquired eosinophilia – 4B03.Z Eosinophilia, unspecified 4B04 Disorders with decreased monocyte counts 4B05 Disorders with increased monocyte counts 4B06 Acquired lymphopenia 4B07 Acquired lymphocytosis 4B0Y Other specified immune system disorders involving white cell lineages 4B0Z Immune system disorders involving white cell lineages, unspecified 4B20 Sarcoidosis – 4B20.0 Sarcoidosis of lung – 4B20.1 Sarcoidosis of lymph nodes – 4B20.2 Sarcoidosis of the digestive system – 4B20.3 Neurosarcoidosis – 4B20.4 Ocular sarcoidosis – 4B20.5 Cutaneous sarcoidosis – 4B20.Y Other specified sarcoidosis – 4B20.Z Sarcoidosis, unspecified 4B21 Polyclonal hypergammaglobulinaemia 4B22 Cryoglobulinaemia 4B23 Immune reconstitution inflammatory syndrome 4B24 Graft-versus-host disease – 4B24.0 Acute graft-versus-host disease – 4B24.1 Chronic graft-versus-host disease – 4B24.Y Other specified graft-versus-host disease – 4B24.Z Graft-versus-host disease, unspecified 4B2Y Other specified disorders involving the immune system 4B40 Diseases of thymus 4B40.0 Persistent hyperplasia of thymus 4B40.1 Abscess of thymus 4B40.2 Good syndrome 4B40.Y Other specified diseases of thymus 4B40.Z Diseases of thymus, unspecified – FA00 Osteoarthritis of hip –– FA00.0 Primary osteoarthritis of hip –– FA00.1 Post traumatic osteoarthritis of hip –– FA00.2 Other secondary osteoarthritis of hip –– FA00.Z Osteoarthritis of hip, unspecified – FA01 Osteoarthritis of knee –– FA01.0 Primary osteoarthritis of knee –– FA01.1 Post traumatic osteoarthritis of knee –– FA01.2 Other secondary osteoarthritis of knee –– FA01.Z Osteoarthritis of knee, unspecified – FA02 Osteoarthritis of wrist or hand –– FA02.0 Primary osteoarthritis of wrist or hand –– FA02.1 Post traumatic osteoarthritis of wrist or hand –– FA02.2 Other secondary osteoarthritis of wrist or hand –– FA02.Z Osteoarthritis of wrist or hand, unspecified – FA03 Osteoarthritis of other specified joint –– FA03.0 Primary osteoarthritis of other specified joint –– FA03.1 Post traumatic osteoarthritis of other specified joint –– FA03.2 Other secondary osteoarthritis of other specified joint –– FA03.Z Osteoarthritis of other specified joint, unspecified – FA04 Oligoosteoarthritis – FA05 Polyosteoarthritis – FA0Z Osteoarthritis, unspecified – FA10 Direct infections of joint –– FA10.0 Bacterial infection of joint –– FA10.1 Viral infection of joint –– FA10.2 Fungal infection of joint –– FA10.Z Direct infections of joint, unspecified – FA11 Reactive arthropathies –– FA11.0 Arthropathy following intestinal bypass –– FA11.1 Arthropathy following vaccination –– FA11.2 Arthropathy following genitourinary infection –– FA11.Y Other specified reactive arthropathies –– FA11.Z Reactive arthropathies, unspecified – FA12 Postinfectious arthropathies –– FA12.0 Bacterial postinfectious arthropathy –– FA12.1 Viral postinfectious arthropathies –– FA12.2 Fungal postinfectious arthropathies –– FA12.3 Parasitic postinfectious arthropathies –– FA12.Y Other specified postinfectious arthropathies –– FA12.Z Postinfectious arthropathies, unspecified – FA13 Infectious spondyloarthritis – FA1Y Other specified infection related arthropathies – FA1Z Infection related arthropathies, unspecified – FA20 Rheumatoid arthritis –– FA20.0 Seropositive rheumatoid arthritis –– FA20.1 Seronegative rheumatoid arthritis –– FA20.Z Rheumatoid arthritis, serology unspecified – FA21 Psoriatic arthritis –– FA21.0 Psoriatic spondyloarthritis –– FA21.Y Other specified psoriatic arthritis –– FA21.Z Psoriatic arthritis, unspecified – FA22 Polymyalgia rheumatica – FA23 Adult-onset Still disease – FA24 Juvenile idiopathic arthritis –– FA24.0 Juvenile idiopathic oligoarthritis –– FA24.1 Juvenile idiopathic polyarthritis –– FA24.2 Juvenile psoriatic arthritis –– FA24.3 Juvenile enthesitis related arthritis –– FA24.4 Juvenile systemic arthritis –– FA24.Y Other specified juvenile idiopathic arthritis –– FA24.Z Juvenile idiopathic arthritis, unspecified ––– FA24.00 Juvenile idiopathic oligoarthritis, onset persistent ––– FA24.01 Juvenile idiopathic oligoarthritis, onset extended ––– FA24.0Z Juvenile idiopathic oligoarthritis, onset unspecified – FA25 Gout –– FA25.0 Primary gout –– FA25.1 Secondary gout –– FA25.2 Gout without specification whether primary or secondary ––– FA25.10 Lead-induced gout ––– FA25.11 Drug-induced gout ––– FA25.12 Gouty arthropathy due to enzyme defects or other inherited disorders ––– FA25.1Y Other specified secondary gout ––– FA25.1Z Secondary gout, unspecified ––– FA25.20 Tophaceous gout ––– FA25.2Y Other specified gout without specification whether primary or secondary ––– FA25.2Z Gout, unspecified – FA26 Certain specified crystal arthropathies –– FA26.0 Calcium pyrophosphate dehydrate deposition disease –– FA26.1 Hydroxyapatite deposition disease –– FA26.2 Chondrocalcinosis –– FA26.Y Other specified crystal arthropathies –– FA26.Z Crystal arthropathies, unspecified – FA27 Certain specified inflammatory arthropathies –– FA27.0 Kashin-Beck disease –– FA27.1 Pigmented villonodular synovitis –– FA27.2 Palindromic rheumatism –– FA27.3 Transient synovitis –– FA27.4 Intermittent hydrarthrosis –– FA27.Y Other specified inflammatory arthropathies – FA2Z Inflammatory arthropathies, unspecified – FA30 Acquired deformities of fingers or toes –– FA30.0 Acquired hallux valgus –– FA30.1 Hallux rigidus –– FA30.2 Acquired hammer toe –– FA30.Y Other specified acquired deformities of fingers or toes –– FA30.Z Acquired deformities of fingers or toes, unspecified – FA31 Other acquired deformities of limbs –– FA31.0 Valgus deformity, not elsewhere classified –– FA31.1 Varus deformity, not elsewhere classified –– FA31.2 Flexion deformity –– FA31.3 Acquired wrist drop –– FA31.4 Acquired foot drop –– FA31.5 Acquired pes planus –– FA31.6 Acquired clawhand or clubhand –– FA31.7 Acquired clawfoot or clubfoot –– FA31.8 Acquired unequal limb length –– FA31.Y Other specified acquired deformities of limbs –– FA31.Z Acquired deformities of limbs, unspecified – FA32 Disorders of patella –– FA32.0 Recurrent instability of patella –– FA32.1 Patellofemoral disorders –– FA32.Y Other specified disorders of patella –– FA32.Z Disorders of patella, unspecified – FA33 Internal derangement of knee –– FA33.0 Cystic meniscus –– FA33.1 Discoid meniscus –– FA33.2 Derangement of meniscus due to old tear or injury –– FA33.3 Loose body in knee –– FA33.4 Chronic instability of knee –– FA33.Y Other specified internal derangement of knee –– FA33.Z Internal derangement of knee, unspecified ––– FA33.40 Chronic instability of knee, medial collateral ligament or other or unspecified part of medial meniscus ––– FA33.4Y Other specified chronic instability of knee ––– FA33.4Z Chronic instability of knee, unspecified – FA34 Certain specified joint derangements –– FA34.0 Loose body in joint –– FA34.1 Disorder of ligament –– FA34.2 Recurrent instability of joint –– FA34.3 Contracture of joint –– FA34.4 Ankylosis of joint –– FA34.5 Impingement syndrome of hip –– FA34.Y Other joint derangements – FA35 Wear of articular bearing surface of joint prosthesis –– FA35.0 Wear of articular bearing surface of joint prosthesis of hip –– FA35.1 Wear of articular bearing surface of joint prosthesis of knee –– FA35.2 Wear of articular bearing surface of joint prosthesis of other joint –– FA35.Z Wear of articular bearing surface of joint prosthesis of unspecified joint – FA36 Effusion of joint –– FA36.0 Effusion of joint containing blood –– FA36.Y Other specified effusion of joint –– FA36.Z Effusion of joint, unspecified – FA37 Certain joint disorders, not elsewhere classified –– FA37.0 Osteophyte –– FA37.Y Other specified certain joint disorders, not elsewhere classified –– FA37.Z Certain joint disorders, not elsewhere classified, unspecified – FA38 Arthropathy in diseases classified elsewhere –– FA38.0 Diabetic arthropathy –– FA38.1 Neuropathic arthropathy –– FA38.2 Arthropathy in hypersensitivity reactions classified elsewhere –– FA38.3 Haemophilic arthropathy –– FA38.Y Other specified arthropathy in diseases classified elsewhere –– FA38.Z Unspecified arthropathy in diseases classified elsewhere ––– FA38.10 Diabetic Charcot arthropathy ––– FA38.1Y Other specified neuropathic arthropathy ––– FA38.1Z Neuropathic arthropathy, unspecified – FA3Z Unspecified joint disorders and deformities of limbs FA5Y Other specified arthropathies FA5Z Arthropathies, unspecified – FA70 Spinal deformities –– FA70.0 Kyphosis –– FA70.1 Scoliosis –– FA70.2 Lordosis –– FA70.Z Spinal deformities, unspecified – FA71 Torticollis – FA72 Disorders of vertebra –– FA72.0 Ankylosing hyperostosis –– FA72.1 Kissing spine –– FA72.2 Traumatic spondylopathy –– FA72.3 Fatigue fracture of vertebra –– FA72.4 Collapsed vertebra, not elsewhere classified –– FA72.Y Other specified disorders of vertebra –– FA72.Z Disorders of vertebra, unspecified – FA7Y Other specified structural disorders of spine – FA7Z Structural disorders of spine, unspecified – FA80 Intervertebral disc degeneration –– FA80.0 Intervertebral disc degeneration of cervical spine without prolapsed disc –– FA80.1 Intervertebral disc degeneration of cervical spine with prolapsed disc –– FA80.2 Intervertebral disc degeneration of cervical spine with bony spur at the vertebra –– FA80.3 Intervertebral disc degeneration of cervical spine with nervous system involvement –– FA80.4 Intervertebral disc degeneration of thoracic spine without prolapsed disc –– FA80.5 Intervertebral disc degeneration of thoracic spine with prolapsed disc –– FA80.6 Intervertebral disc degeneration of thoracic spine with bony spur at the vertebra –– FA80.7 Intervertebral disc degeneration of thoracic spine with nervous system involvement –– FA80.8 Intervertebral disc degeneration of lumbar spine without prolapsed disc –– FA80.9 Intervertebral disc degeneration of lumbar spine with prolapsed disc –– FA80.A Intervertebral disc degeneration of lumbar spine with bony spur at the vertebra –– FA80.B Intervertebral disc degeneration of lumbar spine with nervous system involvement –– FA80.Y Other specified intervertebral disc degeneration –– FA80.Z Intervertebral disc degeneration, unspecified – FA81 Spondylolysis –– FA81.0 Spondylolysis with slippage –– FA81.1 Spondylolysis without slippage –– FA81.Z Spondylolysis, unspecified – FA82 Spinal stenosis – FA83 Ossification of spinal ligaments – FA84 Spondylolisthesis –– FA84.0 Spondylolisthesis with pars defect –– FA84.1 Spondylolisthesis without pars defect –– FA84.Z Spondylolisthesis, unspecified – FA85 Spinal endplate defects –– FA85.0 Spinal epiphysiopathy with no determinant –– FA85.1 Spinal epiphysiopathy with determinants –– FA85.Y Other specified spinal endplate defects –– FA85.Z Spinal endplate defects, unspecified ––– FA85.10 Localised central endplate defect ––– FA85.11 Multiple anterior endplate defect ––– FA85.12 Separation of ring apophysis ––– FA85.1Y Other specified spinal epiphysiopathy with determinants ––– FA85.1Z Spinal epiphysiopathy with determinants, unspecified – FA8Y Other specified degenerative condition of spine – FA8Z Degenerative condition of spine, unspecified – FA90 Infection of vertebra –– FA90.0 Infection of vertebra with no determinant –– FA90.1 Infection of vertebra with determinants –– FA90.Y Other specified infection of vertebra –– FA90.Z Infection of vertebra, unspecified – FA91 Infection of intervertebral disc – FA92 Inflammatory spondyloarthritis –– FA92.0 Axial spondyloarthritis –– FA92.1 Peripheral spondyloarthritis –– FA92.Y Other specified inflammatory spondyloarthritis –– FA92.Z Inflammatory spondyloarthritis, unspecified ––– FA92.00 Spinal enthesitis ––– FA92.01 Sacroiliitis, not elsewhere classified ––– FA92.0Y Other specified axial spondyloarthritis ––– FA92.0Z Axial spondyloarthritis, unspecified – FA9Y Other specified inflammation of spine – FA9Z Inflammation of spine, unspecified – FB00 Ankylosis of spinal joint – FB0Y Other specified spondylopathies – FB0Z Spondylopathies, unspecified FB10 Spinal instabilities FB1Y Other specified conditions associated with the spine FB1Z Conditions associated with the spine, unspecified – FB30 Infectious myositis – FB31 Calcification or ossification of muscle –– FB31.0 Progressive osseous heteroplasia –– FB31.1 Fibrodysplasia ossificans progressiva –– FB31.Y Other specified calcification or ossification of muscle –– FB31.Z Calcification or ossification of muscle, unspecified – FB32 Certain specified disorders of muscle –– FB32.0 Diastasis of muscle –– FB32.1 Spontaneous rupture of muscle –– FB32.2 Ischaemic infarction of muscle –– FB32.3 Immobility syndrome –– FB32.4 Contracture of muscle –– FB32.5 Muscle strain or sprain –– FB32.Y Other specified disorders of muscles ––– FB32.20 Idiopathic rhabdomyolysis ––– FB32.2Y Other specified ischaemic infarction of muscle ––– FB32.2Z Ischaemic infarction of muscle, unspecified – FB33 Secondary disorders of muscle – FB3Z Disorders of muscles, unspecified – FB40 Tenosynovitis –– FB40.0 Infectious tenosynovitis –– FB40.1 Plantar fasciitis –– FB40.2 Posterior tibial tendonitis –– FB40.3 Calcific tendinitis –– FB40.4 Trigger finger –– FB40.5 Radial styloid tenosynovitis –– FB40.Y Other specified tenosynovitis –– FB40.Z Tenosynovitis, unspecified – FB41 Spontaneous rupture of synovium or tendon –– FB41.0 Spontaneous rupture of popliteal cyst –– FB41.1 Spontaneous rupture of synovium –– FB41.2 Spontaneous rupture of tendon –– FB41.Y Other specified spontaneous rupture of synovium or tendon –– FB41.Z Spontaneous rupture of synovium or tendon, unspecified – FB42 Certain specified disorders of synovium or tendon –– FB42.0 Acquired short Achilles tendon –– FB42.1 Contracture of tendon sheath –– FB42.2 Ganglion –– FB42.3 Synovial hypertrophy, not elsewhere classified – FB43 Secondary disorders of synovium or tendon – FB4Y Other specified disorders of synovium or tendon – FB4Z Disorders of synovium or tendon, unspecified – FB50 Bursitis –– FB50.0 Infectious bursitis –– FB50.1 Bursitis related to use, overuse or pressure –– FB50.2 Synovial cyst of popliteal space –– FB50.3 Calcium deposit in bursa –– FB50.Y Other specified bursitis –– FB50.Z Bursitis, unspecified – FB51 Fibroblastic disorders –– FB51.0 Palmar fascial fibromatosis –– FB51.1 Knuckle pads –– FB51.2 Fasciitis and fibromatosis –– FB51.3 Fibroblastic rheumatism –– FB51.4 Retroperitoneal fibrosis –– FB51.Y Other specified fibroblastic disorders –– FB51.Z Fibroblastic disorders, unspecified ––– FB51.40 Primary retroperitoneal fibrosis ––– FB51.4Y Other specified retroperitoneal fibrosis ––– FB51.4Z Retroperitoneal fibrosis, unspecified – FB52 Soft tissue disorders in diseases classified elsewhere – FB53 Shoulder lesions –– FB53.0 Adhesive capsulitis of shoulder –– FB53.1 Rotator cuff syndrome –– FB53.2 Impingement syndrome of shoulder –– FB53.Y Other specified shoulder lesions –– FB53.Z Shoulder lesions, unspecified – FB54 Enthesopathies of lower limb –– FB54.0 Iliac crest spur –– FB54.1 Iliotibial band syndrome –– FB54.2 Tibial collateral bursitis –– FB54.3 Calcaneal spur –– FB54.4 Metatarsalgia –– FB54.Y Other specified enthesopathies of lower limb –– FB54.Z Enthesopathies of lower limb, unspecified – FB55 Certain specified enthesopathies –– FB55.0 Medial epicondylitis of elbow –– FB55.1 Lateral epicondylitis of elbow –– FB55.2 Periarthritis of wrist –– FB55.Z Enthesopathies, unspecified – FB56 Specified soft tissue disorders, not elsewhere classified –– FB56.0 Foreign body granuloma of soft tissue, not elsewhere classified –– FB56.1 Residual foreign body in soft tissue –– FB56.2 Myalgia –– FB56.3 Hypertrophy of infrapatellar fat pad –– FB56.4 Pain in limb –– FB56.6 Other specified soft tissue disorders FB6Z Soft tissue disorders, unspecified FB80 Certain specified disorders of bone density or structure – FB80.0 Fibrous dysplasia of bone – FB80.1 Skeletal fluorosis – FB80.2 Osteitis condensans – FB80.3 Hyperostosis of skull – FB80.4 Osteosclerosis – FB80.5 Solitary bone cyst – FB80.6 Aneurysmal bone cyst – FB80.7 Malunion of fracture – FB80.8 Nonunion of fracture – FB80.9 Delayed union of fracture – FB80.A Stress fracture, not elsewhere classified – FB80.B Pathological fracture – FB80.Y Other specified disorders of bone density and structure – FB80.Z Disorder of bone density and structure, unspecified FB81 Osteonecrosis – FB81.0 Idiopathic aseptic osteonecrosis – FB81.1 Osteonecrosis due to dialysis – FB81.2 Drug-induced osteonecrosis – FB81.3 Osteonecrosis due to trauma – FB81.4 Osteonecrosis due to haemoglobinopathy – FB81.5 Osteonecrosis due to ionizing radiation – FB81.6 Alcohol induced osteonecrosis – FB81.Y Other specified osteonecrosis – FB81.Z Osteonecrosis, unspecified FB82 Chondropathies – FB82.0 Chondromalacia – FB82.1 Osteochondrosis or osteochondritis dissecans – FB82.2 Slipped upper femoral epiphysis – FB82.3 Relapsing polychondritis – FB82.Y Other specified chondropathies – FB82.Z Chondropathies, unspecified –– FB82.00 Chondromalacia patellae –– FB82.0Y Other specified chondromalacia –– FB82.0Z Chondromalacia, unspecified FB83 Low bone mass disorders – FB83.0 Osteopenia – FB83.1 Osteoporosis – FB83.2 Adult osteomalacia –– FB83.00 Premenopausal idiopathic osteopenia –– FB83.01 Postmenopausal osteopenia –– FB83.02 Senile osteopenia –– FB83.03 Osteopenia of disuse –– FB83.04 Drug-induced osteopenia –– FB83.0Y Other specified osteopenia –– FB83.0Z Osteopenia, unspecified –– FB83.10 Premenopausal idiopathic osteoporosis –– FB83.11 Postmenopausal osteoporosis –– FB83.12 Osteoporosis of disuse –– FB83.13 Drug-induced osteoporosis –– FB83.14 Osteoporosis due to malabsorption –– FB83.1Y Other specified osteoporosis –– FB83.1Z Osteoporosis, unspecified –– FB83.20 Aluminium bone disease –– FB83.21 Adult osteomalacia due to malnutrition –– FB83.22 Drug-induced adult osteomalacia –– FB83.2Y Other specified adult osteomalacia –– FB83.2Z Adult osteomalacia, unspecified FB84 Osteomyelitis or osteitis – FB84.0 Acute haematogenous osteomyelitis – FB84.1 Other acute osteomyelitis – FB84.2 Subacute osteomyelitis – FB84.3 Chronic multifocal osteomyelitis – FB84.4 Chronic osteomyelitis with draining sinus – FB84.5 Other chronic haematogenous osteomyelitis – FB84.Y Other specified osteomyelitis or osteitis – FB84.Z Osteomyelitis or osteitis, unspecified FB85 Paget disease of bone – FB85.0 Juvenile Paget disease – FB85.1 Paget disease of bone in neoplastic disease – FB85.Y Other specified Paget disease of bone – FB85.Z Paget disease of bone, unspecified FB86 Disorders associated with bone growth – FB86.0 Epiphyseal arrest – FB86.1 Bone hyperplasias – FB86.2 Osteolysis – FB86.Y Other specified disorders associated with bone growth – FB86.Z Disorders associated with bone growth, unspecified –– FB86.10 Hypertrophic osteoarthropathy –– FB86.11 Hypertrophy of bone –– FB86.1Y Other specified bone hyperplasias –– FB86.1Z Bone hyperplasias, unspecified FB8Y Other specified osteopathies or chondropathies FB8Z Osteopathies or chondropathies, unspecified FC00 Certain specified acquired deformities of musculoskeletal system or connective tissue, not elsewhere classified FC00.0 Acquired deformity of nose FC00.1 Acquired deformity of neck FC00.2 Acquired deformity of chest or rib FC00.3 Acquired deformity of pelvis FC00.4 Acquired deformity of trunk FC00.Y Acquired deformities of musculoskeletal system and connective tissue, not classified elsewhere, other specified sites FC01 Postprocedural disorders of the musculoskeletal system FC01.0 Pseudarthrosis after fusion or arthrodesis FC01.1 Postlaminectomy syndrome, not elsewhere classified FC01.2 Post radiation kyphosis FC01.3 Postlaminectomy kyphosis FC01.4 Postsurgical lordosis FC01.5 Post radiation scoliosis FC01.6 Fracture of bone following insertion of orthopaedic implant, joint prosthesis, or bone plate FC01.7 Nonunion after arthrodesis FC01.8 Postsurgical osteolysis FC01.9 Postoophorectomy osteoporosis FC01.A Postsurgical malabsorption osteoporosis – FC01.70 Nonunion after spinal arthrodesis – FC01.7Y Nonunion after arthrodesis of other sites FC0Y Other specified diseases of the musculoskeletal system or connective tissue FC0Z Diseases of the musculoskeletal system or connective tissue, unspecified
synonyms Secondary Sjögren syndrome
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