Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
M31 Other necrotizing vasculopathies M31.0 Hypersensitivity angiitis Goodpasture's syndrome M31.1 Thrombotic microangiopathy Thrombotic thrombocytopenic purpura M31.2 Lethal midline granuloma M31.3 Wegener's granulomatosis Necrotizing respiratory granulomatosis M31.4 Aortic arch syndrome [Takayasu] M31.5 Giant cell arteritis with polymyalgia rheumatica M31.6 Other giant cell arteritis M31.7 Microscopic polyangiitis Microscopic polyarteritis Excludes: polyarteritis nodosa (M30.0) M31.8 Other specified necrotizing vasculopathies Hypocomplementaemic vasculitis M31.9 Necrotizing vasculopathy, unspecified M32 Systemic lupus erythematosus Excludes: lupus erythematosus (discoid)(NOS) ( L93.0 ) M32.0 Drug-induced systemic lupus erythematosus Use additional external cause code (Chapter XX), if desired, to identify drug. M32.1† Systemic lupus erythematosus with organ or system involvement Libman-Sacks disease ( I39.-* ) Lupus pericarditis ( I32.8* ) Systemic lupus erythematosus with: · kidney involvement ( N08.5* , N16.4* ) · lung involvement ( J99.1* ) M32.8 Other forms of systemic lupus erythematosus M32.9 Systemic lupus erythematosus, unspecified M33 Dermatopolymyositis M33.0 Juvenile dermatomyositis M33.1 Other dermatomyositis M33.2 Polymyositis M33.9 Dermatopolymyositis, unspecified M34 Systemic sclerosis Includes: scleroderma Excludes: scleroderma: · circumscribed ( L94.0 ) · neonatal ( P83.8 ) M34.0 Progressive systemic sclerosis 420 WHO’s ICD-10
M34.1 CR(E)ST syndrome Combination of calcinosis, Raynaud's phenomenon, (o)esophageal dysfunction, sclerodactyly, telangiectasia. M34.2 Systemic sclerosis induced by drugs and chemicals Use additional external cause code (Chapter XX), if desired, to identify cause. M34.8 Other forms of systemic sclerosis Systemic sclerosis with: · lung involvement† ( J99.1* ) · myopathy† ( G73.7* ) M34.9 Systemic sclerosis, unspecified M35 Other systemic involvement of connective tissue Excludes: reactive perforating collagenosis ( L87.1 ) M35.0 Sicca syndrome [Sjögren] Sjögren's syndrome with: · keratoconjunctivitis† ( H19.3* ) · lung involvement† ( J99.1* ) · myopathy† ( G73.7* ) · renal tubulo-interstitial disorders† ( N16.4* ) M35.1 Other overlap syndromes Mixed connective tissue disease Excludes: polyangiitis overlap syndrome ( M30.8 ) M35.2 Behçet's disease M35.3 Polymyalgia rheumatica Excludes: polymyalgia rheumatica with giant cell arteritis ( M31.5 ) M35.4 Diffuse (eosinophilic) fasciitis M35.5 Multifocal fibrosclerosis M35.6 Relapsing panniculitis [Weber-Christian] Excludes: panniculitis: · NOS ( M79.3 ) · lupus ( L93.2 ) M35.7 Hypermobility syndrome Familial ligamentous laxity Excludes: Ehlers-Danlos syndrome ( Q79.6 ) ligamentous laxity NOS ( M24.2 ) M35.8 Other specified systemic involvement of connective tissue M35.9 Systemic involvement of connective tissue, unspecified Autoimmune disease (systemic) NOS Collagen (vascular) disease NOS M36* Systemic disorders of connective tissue in diseases classified elsewhere Excludes: arthropathies in diseases classified elsewhere ( M14.-* ) M36.0* Dermato(poly)myositis in neoplastic disease ( C00-D48† ) Version for 2007 421
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M34.1 CR(E)ST syndrome<br />
Combination of calcinosis, Raynaud's phenomenon, (o)esophageal dysfunction,<br />
sclerodactyly, telangiectasia.<br />
M34.2 Systemic sclerosis induced by drugs <strong>and</strong> chemicals<br />
Use additional external cause code (Chapter XX), if desired, to identify cause.<br />
M34.8 Other forms of systemic sclerosis<br />
Systemic sclerosis with:<br />
· lung involvement† ( J99.1* )<br />
· myopathy† ( G73.7* )<br />
M34.9 Systemic sclerosis, unspecified<br />
M35<br />
Other systemic involvement of connective tissue<br />
Excludes: reactive perforating collagenosis ( L87.1 )<br />
M35.0 Sicca syndrome [Sjögren]<br />
Sjögren's syndrome with:<br />
· keratoconjunctivitis† ( H19.3* )<br />
· lung involvement† ( J99.1* )<br />
· myopathy† ( G73.7* )<br />
· renal tubulo-interstitial disorders† ( N16.4* )<br />
M35.1 Other overlap syndromes<br />
Mixed connective tissue disease<br />
Excludes: polyangiitis overlap syndrome ( M30.8 )<br />
M35.2 Behçet's disease<br />
M35.3 Polymyalgia rheumatica<br />
Excludes: polymyalgia rheumatica with giant cell arteritis ( M31.5 )<br />
M35.4 Diffuse (eosinophilic) fasciitis<br />
M35.5 Multifocal fibrosclerosis<br />
M35.6 Relapsing panniculitis [Weber-Christian]<br />
Excludes: panniculitis:<br />
· NOS ( M79.3 )<br />
· lupus ( L93.2 )<br />
M35.7 Hypermobility syndrome<br />
Familial ligamentous laxity<br />
Excludes: Ehlers-Danlos syndrome ( Q79.6 )<br />
ligamentous laxity NOS ( M24.2 )<br />
M35.8 Other specified systemic involvement of connective tissue<br />
M35.9 Systemic involvement of connective tissue, unspecified<br />
Autoimmune disease (systemic) NOS<br />
Collagen (vascular) disease NOS<br />
M36* Systemic disorders of connective tissue in <strong>diseases</strong> classified<br />
elsewhere<br />
Excludes: arthropathies in <strong>diseases</strong> classified elsewhere ( M14.-* )<br />
M36.0* Dermato(poly)myositis in neoplastic disease ( C00-D48† )<br />
Version for 2007 421