416879000: Scleritis due to granulomatosis with polyangiitis (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Anomaly of eye\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Head finding (finding)\Finding of head region\Globe finding (finding)\Sclera and episclera finding\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Head finding (finding)\Disorder of head (disorder)\Inflammatory disorder of head\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \General finding of soft tissue\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Procedure related finding\Evaluation finding\Measurement finding\...
• \Finding of substance level (finding)\Finding of protein level (finding)\Finding of specific antibody level (finding)\Autoantibody level - finding\Antineutrophil cytoplasmic antibody positive\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Detected by measurement\Antineutrophil cytoplasmic antibody positive\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Eye / vision finding\Globe finding (finding)\Disorder of eye proper (disorder)\Anomaly of eye\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Eye / vision finding\Globe finding (finding)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Eye / vision finding\Globe finding (finding)\Sclera and episclera finding\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Cardiovascular finding\Blood vessel finding\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Anomaly of eye\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of immune function (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of body system\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammatory disorder of head\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of the cardiovascular system\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of sclera\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of head (disorder)\Inflammatory disorder of head\Inflammatory disorder of the eye\Scleritis (disorder)\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Systemic disease\A rare scleritis characterized by severe ocular inflammation of sclera associated with an underlying systemic inflammatory condition, most often rheumatoid arthritis, granulomatosis with polyangiitis, but also seronegative spondyloarthropathies, vasculitides and systemic lupus erythematosus. Ocular presentation is a tender or painful, violet-blueish eye, with injection of deep scleral vessels. It can be unilateral or bilateral. Immune-mediated scleritis is more often granulomatous and/or necrotizing. Systemic clinical signs depend on the underlying disease.\Scleritis due to granulomatosis with polyangiitis
• \Disease\Systemic disease\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Systemic disease\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Vasculitis due to systemic disease\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Primary systemic vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Inflammation of systemic vasculature (disorder)\Secondary systemic vasculitis\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Small vessel vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis
• \Disease\Disorder of soft tissue\Disorder of blood vessel (disorder)\Vasculitis (disorder)\Antineutrophil cytoplasmic antibody positive vasculitis (disorder)\Wegener's granulomatosis (disorder)\Scleritis due to granulomatosis with polyangiitis

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jun 2024. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3754209010	Scleritis due to granulomatosis with polyangiitis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3754210017	Scleritis due to granulomatosis with polyangiitis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2547089019	Scleritis due to Wegener granulomatosis (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2549415019	Scleritis due to Wegener granulomatosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2553973014	Scleritis due to Wegener's granulomatosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3754209010	Scleritis due to granulomatosis with polyangiitis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3754210017	Scleritis due to granulomatosis with polyangiitis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
535901000274117	Skleritis verursacht durch Granulomatose mit Polyangiitis	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5282501000241115	granulomatose avec polyangéite (Wegener) avec sclérite	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5282501000241115	granulomatose avec polyangéite (Wegener) avec sclérite	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
535901000274117	Skleritis verursacht durch Granulomatose mit Polyangiitis	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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