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409774005: Inflammatory morphology (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2465225015 Inflammatory morphology (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2471508012 Inflammatory morphology en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
65551000077117 morphologie d'une inflammation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

197 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Inflammatory morphology (morphologic abnormality) Is a Morphologically abnormal structure true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
A type of primary hypophysitis characterised by an inflammation of the entire pituitary gland. Common clinical presentation is diabetes insipidus with polyuria and polydipsia and partial or panhypopituitarism. Other symptoms may include headaches, nausea/vomiting, visual disturbances and fatigue. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare retinal vasculopathy disease characterized by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations, and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion, retinal neovascularization, and macular exudation, leading to severe, bilateral vision loss. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
A rare retinal vasculopathy disease characterized by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations, and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion, retinal neovascularization, and macular exudation, leading to severe, bilateral vision loss. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A type of primary hypophysitis characterized by an inflammation of the posterior pituitary and the stalk. The major clinical manifestation is diabetes insipidus with polyuria and polydipsia. Less frequent symptoms are headaches, adrenal insufficiency, hyperprolactinemia and hypogonadism. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Encrusted cystitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare, acquired pituitary hormone deficiency, a type of primary hypophysitis characterized by an inflammation of anterior pituitary. Clinical presentation is variable and includes headaches, visual disturbances, symptoms of adrenal insufficiency, hyperprolactinemia, hypothyroidism and hypogonadism. It most commonly affects young women during pregnancy or postpartum period. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare, acquired, demyelinating neuropathy disease characterized by acute, symmetric, monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia, and unsteady gait, as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Osteitis of pelvis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Acute vesicular eczema of foot Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
A group of disorders including ankylosing spondylitis, axial spondylarthritis, spondyloarthritis due to inflammatory bowel disease, and other conditions. They share the common features of inflammation of axial joints, asymmetric oligoarthritis, dactylitis, and enthesitis. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
A group of disorders including ankylosing spondylitis, axial spondylarthritis, spondyloarthritis due to inflammatory bowel disease, and other conditions. They share the common features of inflammation of axial joints, asymmetric oligoarthritis, dactylitis, and enthesitis. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 4
A group of disorders including ankylosing spondylitis, axial spondylarthritis, spondyloarthritis due to inflammatory bowel disease, and other conditions. They share the common features of inflammation of axial joints, asymmetric oligoarthritis, dactylitis, and enthesitis. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A group of disorders including ankylosing spondylitis, axial spondylarthritis, spondyloarthritis due to inflammatory bowel disease, and other conditions. They share the common features of inflammation of axial joints, asymmetric oligoarthritis, dactylitis, and enthesitis. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
A rare, genetic, autoinflammatory syndrome with immune deficiency disease characterized by recurrent and severe flares of generalized pustular psoriasis associated with high fever, asthenia, and systemic inflammation, due to IL36R antagonist deficiency. Psoriatic nail changes (e.g. pitting and onychomadesis) and ichthyosis may occasionally be associated. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Synovitis of ankle joint Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Synovitis of joint of foot Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Neutrophilic dermatosis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Aseptic peritonitis following procedure (disorder) Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Inflammation of large intestine or colon due to exposure to contaminated endoscope or by intentional or accidental administration of enemas containing various chemicals. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Polyneuritis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Neurotrophic keratoconjunctivitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Neurotrophic keratoconjunctivitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Nephritic syndrome Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Panuveitis Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
Panuveitis Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Panuveitis Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 4
Panuveitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
House allergic alveolitis is a hypersensitivity pneumonitis resulting from the inhalation of an antigen to which an individual has been previously sensitized in his/her domestic environment. House allergic alveolitis encompasses summer hypersensitivity pneumonitis, humidifier-induced lung diseases, hot tub lung and legionellosis. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Uncomplicated allergic asthma (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Eczema of male genitalia Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Exacerbation of allergic asthma Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Occupational allergic contact dermatitis caused by systemic drug or medicament Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Occupational allergic contact dermatitis caused by topical medicament Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Sepsis caused by virus (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Vasculitis due to ADA2 deficiency is a rare, genetic, systemic and rheumatologic disease due to adenosine deaminase-2 inactivating mutations, combining variable features of autoinflammation, vasculitis, and a mild immunodeficiency. Variable clinical presentation includes chronic or recurrent systemic inflammation with fever, livedo reticularis or racemosa, early-onset ischaemic or haemorrhagic strokes, peripheral neuropathy, abdominal pain, hepatosplenomegaly, portal hypertension, cutaneous polyarteritis nodosa, variable cytopenia and immunoglobulin deficiency. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Blepharoconjunctivitis of left eye (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Blepharoconjunctivitis of left eye (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Blepharoconjunctivitis of right eye (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Blepharoconjunctivitis of right eye (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Infectious epithelial keratitis is a rare, potentially sight-threatening, acquired ocular disease characterized by corneal epithelium inflammation resulting from viral (mainly Herpes Simplex virus), bacterial, fungal or protist infection, manifesting with variable symptoms, such as conjunctival hyperemia, lacrimation, rapid onset of pain, blurred vision and/or photophobia, depending on the causative agent. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) is a rare, acquired, neurological disease characterized by encephalopathy associated with elevated antithyroid antibodies, in the absence of other causes. Clinical presentation varies from minor cognitive impairment to status epilepticus and coma, and frequently includes seizures, confusion, speech disorder, memory impairment, ataxia and psychiatric manifestations. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) is a rare, acquired, neurological disease characterized by encephalopathy associated with elevated antithyroid antibodies, in the absence of other causes. Clinical presentation varies from minor cognitive impairment to status epilepticus and coma, and frequently includes seizures, confusion, speech disorder, memory impairment, ataxia and psychiatric manifestations. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Limbic encephalitis with contactin-associated protein-like 2 antibodies (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Mycoplasma encephalitis is a rare infectious encephalitis characterized by an acute onset of neurological signs and symptoms (e.g. altered consciousness, seizures, headaches, meningeal signs, behavioral changes) due to bacterial infection by Mycoplasma pneumoniae. Patients typically present unspecific signs and symptoms, such as fever, nausea, vomiting, fatigue, prior to onset of neurological manifestations and frequently have a history of a respiratory tract infection (e.g. pneumonia, bronchiolitis, pharyngitis). Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Non-herpetic acute limbic encephalitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare genetic autoinflammatory syndrome characterized by early-onset of repeated episodes of fever, nodular neutrophil-rich panniculitis, arthralgia, and lipodystrophy. Additional reported features include diarrhea, failure to thrive, lymphadenopathy, and vasculitis. Laboratory examination may reveal elevated serum C-reactive protein and leukocytosis with neutrophilia in the absence of infection. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Radionuclide imaging of whole body using gallium-67 for localization of inflammation (procedure) Direct morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Steatohepatitis caused by ingestible alcohol Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare neurologic disorder characterized by a unique non-REM and REM parasomnia with sleep breathing dysfunction, gait instability and repetitive episodes of respiratory insufficiency, as well as autoantibodies against IgLON5. Patients may present stridor, chorea, limb ataxia, abnormal ocular movements, and bulbar symptoms (i.e. dysphagia, dysarthria, episodic central hypoventilation) with normal brain MRI. Excessive day sleepiness and cognitive deterioration have also been reported. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare variant of Guillain-Barré syndrome characterized by acute onset monophasic sensory neuropathy with diminished or absent tendon reflexes, loss of proprioception, positive Romberg sign and nerve conduction features of demyelination. It presents several weeks after acute infection with paresthesias, ataxia and neuropathic pain. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Marburg acute multiple sclerosis is a rare variant of multiple sclerosis characterized by a rapidly progressive, aggressive form of multiple sclerosis with numerous large multifocal demyelinating lesions in deep white matter on cerebral MRI that usually leads to severe disability or death within weeks to months without remission. A relapsing form of multiple sclerosis is observed in surviving patients. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 4
Lowe-Kohn-Cohen syndrome is an extremely rare anorectal malformation syndrome characterized by imperforate anus, closed ano-perineal fistula, preauricular skin tag and absent renal abnormalities and pre-axial limb deformities. There have been no further descriptions in the literature since 1983. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Idiopathic recurrent pericarditis is a rare autoinflammatory syndrome defined as recurrence of pericardial inflammation of unknown origin following the first episode of acute pericarditis and a symptom-free interval of 4-6 weeks or longer. Recurrent attacks of chest pain may be the sole presentation or the chest pain may be accompanied by pericardial friction rub, electrocardiographic or echocardiographic changes, pericardial effusion and increased C-reactive protein. Cardiac tamponade is a rare, life-threatening complication. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Paraparetic variant of Guillain-Barré syndrome is a rare variant of Guillain-Barré syndrome characterized by isolated leg weakness, areflexia and radicular leg pain that may simulate a cauda equina or spinal cord syndrome. The arms, ocular, facial, and oropharyngeal muscles are spared, and sphincteric function is normal. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Idiopathic panuveitis is a rare inflammatory eye disease, of unknown etiology, characterized by generalized inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic, unilateral or bilateral visual impairment and ocular discomfort or pain. Patients present an increased risk of development of cataracts, secondary glaucoma, cystoid macular edema and/or retinal detachment. It could potentially result in vision loss. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
Idiopathic panuveitis is a rare inflammatory eye disease, of unknown etiology, characterized by generalized inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic, unilateral or bilateral visual impairment and ocular discomfort or pain. Patients present an increased risk of development of cataracts, secondary glaucoma, cystoid macular edema and/or retinal detachment. It could potentially result in vision loss. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Idiopathic panuveitis is a rare inflammatory eye disease, of unknown etiology, characterized by generalized inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic, unilateral or bilateral visual impairment and ocular discomfort or pain. Patients present an increased risk of development of cataracts, secondary glaucoma, cystoid macular edema and/or retinal detachment. It could potentially result in vision loss. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Idiopathic panuveitis is a rare inflammatory eye disease, of unknown etiology, characterized by generalized inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic, unilateral or bilateral visual impairment and ocular discomfort or pain. Patients present an increased risk of development of cataracts, secondary glaucoma, cystoid macular edema and/or retinal detachment. It could potentially result in vision loss. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 4
Eosinophilic inflammation Is a True Inflammatory morphology (morphologic abnormality) Inferred relationship Some
Iritis of right eye due to diabetes mellitus (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Iritis of left eye due to diabetes mellitus Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Bilateral iritis due to diabetes mellitus Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Bilateral iritis due to diabetes mellitus Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
A rare immune dysregulation disease with immunodeficiency characterized by severe, progressive infantile onset inflammatory bowel disease with pancolitis, perianal disease (ulceration, fistulae), recurrent respiratory, genitourinary and cutaneous infections, arthritis and a high risk of B-cell lymphoma. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
A rare immune dysregulation disease with immunodeficiency characterized by severe, progressive infantile onset inflammatory bowel disease with pancolitis, perianal disease (ulceration, fistulae), recurrent respiratory, genitourinary and cutaneous infections, arthritis and a high risk of B-cell lymphoma. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Meningitis due to and following central neuraxial nerve block (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Posttransplant acute limbic encephalitis is a rare, acquired, non-paraneoplastic limbic encephalitis disorder, that develops in the setting of treatment-related immunosuppression, typically after allogeneic hemapoietic stem cell transplantation, characterized by onset of confusion, headache, anterograde amnesia, seizures and/or loss of consciousness 2-6 weeks following transplantation. Bilateral, non-enhancing T2 hyperintensities in limbic structures are observed on magnetic resonance imaging. Mild cerebrospinal fluid pleocytosis and syndrome of inappropriate antidiuretic hormone secretion may also be associated. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 4
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 5
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 6
A rare granulomatous autoinflammatory syndrome characterized by infantile-onset, widespread, chronic, recurrent, progressive, lobular panniculitis associated with panuveitis, arthritis and severe systemic granulomatous inflammation. Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 7
Limbic encephalitis with dipeptidyl-peptidase 6 antibodies (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Sterile multifocal osteomyelitis with periostitis and pustulosis is a rare, severe, genetic autoinflammatory syndrome characterized by usually neonatal onset of generalized neutrophilic cutaneous pustulosis and severe, recurrent, multifocal, aseptic osteomyelitis with marked periostitis, typically affecting distal ribs, long bones and vertebral bodies. High levels of acute-phase reactants (with no fever associated) and onychosis are frequently observed additional features. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Interstitial granulomatous dermatitis with arthritis is a rare rheumatologic disease characterized by the occurrence of inflammatory arthritis in association with large, erythematous, symmetrical cutaneous lesions (ranging from typical, but infrequent, cord-like lesions on the flanks to more common violaceous plaques on the trunk and limbs) featuring a typical histologic infiltrate mainly constituted of histiocytes. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Bursitis of right hip (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Bursitis of left hip (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Idiopathic posterior uveitis is a rare, potentially sight-threatening, ocular disease, not attributed to any specific ocular or systemic cause, characterized by focal, multifocal or diffuse non-infectious inflammation in the posterior uvea (i.e. choroiditis, chorioretinitis, retinitis and neuroretinitis). Visual morbidity due to complications (including cystoid macular edema and choroidal neovascularization) has been reported. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Idiopathic linear interstitial keratitis is a rare, acquired ocular disease characterized by migratory or non-migratory, horizontal, linear, stromal infiltrates that may heal spontaneously. Minimal vascularization and scarring may be observed but vision loss is not associated. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare secondary neonatal autoimmune disease characterized by generalized weakness, severe hypotonia, absent or reduced deep tendon reflexes, and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare secondary neonatal autoimmune disease characterized by generalized weakness, severe hypotonia, absent or reduced deep tendon reflexes, and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
A rare neuroinflammatory disease characterized by the onset of ataxia, dysarthria and cerebral white matter changes which are triggered by viral infection. Episodic progressive neurodegeneration (manifesting with loss of motor and verbal skills, muscle weakness, further cerebral white matter degeneration and, eventually, death) is observed in the absence of hematopathology, cytokine overproduction, fever, hypertriglyceridemia, hypofibrinogenemia and hyperferritinemia. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Phlebitis of dorsal venous arch of foot (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Relapsing polychondritis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Endophlebitis of cavernous venous sinus Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Erythema nodosum due to tuberculosis (disorder) Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Endophlebitis of superior sagittal sinus Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Eczema of lower leg (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Mumps orchitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Subdeltoid bursitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Angiocholecystitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Disseminated chorioretinitis Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Disseminated chorioretinitis Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Hereditary tubulointerstitial disorder Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Hereditary tubulointerstitial disorder Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Parainfluenza virus pharyngitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Keratoconjunctivitis sicca, in Sjögren's syndrome Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Keratoconjunctivitis sicca, in Sjögren's syndrome Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
Keratoconjunctivitis sicca, in Sjögren's syndrome Associated morphology False Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2

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