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23583003: Inflammation (morphologic abnormality)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    39603011 Inflammation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    39604017 Leukocytic infiltrate en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    39611018 Inflammatory reaction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    39612013 Inflammatory cell infiltration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    39613015 Inflammatory infiltration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    481656011 Leucocytic infiltrate en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    753120016 Inflammation (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    272051000077118 inflammation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    inflammation Is a Morphologically abnormal structure false Inferred relationship Some
    inflammation Is a Inflammatory morphology (morphologic abnormality) false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Hypertrophic pachymeningitis due to infection (disorder) Associated morphology False inflammation Inferred relationship Some 2
    A rare, brain inflammatory disease characterized by thickening of the dura mater of the cranium or spine with at least two histopathological features of IgG4-related disease: dense lymphoplasmacytic infiltrate, storiform fibrosis, and/or obliterative phlebitis. Patients typically have non-specific CSF findings and might be without systemic involvement or serum IgG4 elevation. Clinical manifestations are caused by mechanical compression of nerve or vascular structure, leading to functional deficit, most commonly headache, cranial nerve palsies, vision problems and motor weakness. Associated morphology False inflammation Inferred relationship Some 1
    Pediatric onset Sjögren syndrome Associated morphology False inflammation Inferred relationship Some 2
    Pediatric onset Sjögren syndrome Associated morphology False inflammation Inferred relationship Some 3
    Lipodermatosclerosis of lower limb due to varicose veins of lower limb Associated morphology False inflammation Inferred relationship Some 11
    Mesenteric adenitis caused by Pasteurella multocida (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Mycobacterial lymphadenitis (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Irritant contact dermatitis caused by dietary substance Associated morphology False inflammation Inferred relationship Some 2
    dermatite allergique de contact causée par un désinfectant Associated morphology False inflammation Inferred relationship Some 2
    Allergic contact dermatitis caused by rubber compound (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Allergic contact dermatitis caused by systemic medicament Associated morphology False inflammation Inferred relationship Some 2
    Irritant contact dermatitis caused by emollient substance Associated morphology False inflammation Inferred relationship Some 1
    Endocarditis of neopulmonary valve Associated morphology False inflammation Inferred relationship Some 2
    Endocarditis of neopulmonary valve Associated morphology False inflammation Inferred relationship Some 3
    Occupational allergic contact dermatitis caused by footwear Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by cosmetic (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by fragrance (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by dental material (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by food flavor Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by food additive Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by hairdressing product Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by agrochemical biocide Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by cutting oil (disorder) Associated morphology False inflammation Inferred relationship Some 2
    dermatite allergique de contact d'origine professionnelle causée par un désinfectant Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by metal compound Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by industrial preservative Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by biocide Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by rubber compound Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by systemic drug or medicament Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by topical medicament Associated morphology False inflammation Inferred relationship Some 2
    Occupational allergic contact dermatitis caused by clothing Associated morphology False inflammation Inferred relationship Some 2
    Allergic contact dermatitis caused by fragrance (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Allergic contact dermatitis caused by footwear (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Allergic contact dermatitis caused by allergenic hapten derived from plant Associated morphology False inflammation Inferred relationship Some 4
    Occupational allergic contact dermatitis caused by allergenic hapten derived from plant Associated morphology False inflammation Inferred relationship Some 4
    Allergic contact dermatitis caused by clothing Associated morphology False inflammation Inferred relationship Some 2
    Scapulothoracic bursitis of right shoulder Associated morphology False inflammation Inferred relationship Some 1
    Scapulothoracic bursitis of left shoulder Associated morphology False inflammation Inferred relationship Some 1
    Saddle sore Associated morphology False inflammation Inferred relationship Some 1
    Limbic encephalitis with contactin-associated protein-like 2 antibodies (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies Associated morphology False inflammation Inferred relationship Some 1
    Bilateral bursitis of ankles Associated morphology False inflammation Inferred relationship Some 2
    Contact dermatitis of external ear (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Rheumatoid arthritis of left shoulder (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Rheumatoid arthritis of right shoulder Associated morphology False inflammation Inferred relationship Some 1
    Retrocalcaneal bursitis of bilateral feet (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Greater trochanteric pain syndrome of bilateral lower limbs (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Medial epicondyle apophysitis due to overuse Associated morphology False inflammation Inferred relationship Some 1
    Bilateral calcaneal apophysitis (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Bilateral calcaneal apophysitis (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Medial epicondyle apophysitis of left elbow due to overuse (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Medial epicondyle apophysitis of right elbow due to overuse (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Allergic contact dermatitis of right lower eyelid (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Allergic contact dermatitis of right eyelid (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Allergic contact dermatitis of left eyelid (disorder) Associated morphology False inflammation 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 False inflammation Inferred relationship Some 1
    Non-herpetic acute limbic encephalitis (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Chronic inflammatory morphology (morphologic abnormality) Is a False inflammation Inferred relationship Some
    Chronic seborrheic otitis externa (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Bilateral bursitis of ankles Associated morphology False inflammation Inferred relationship Some 1
    Retrocalcaneal bursitis of bilateral feet (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Acute seborrheic otitis externa (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Vasculitis with glomerulonephritis Associated morphology False inflammation Inferred relationship Some 2
    Vasculitis with glomerulonephritis Associated morphology False inflammation 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 False inflammation Inferred relationship Some 1
    Influenza with encephalopathy Associated morphology False inflammation Inferred relationship Some 2
    Radionuclide imaging of whole body using gallium-67 for localization of inflammation (procedure) Direct morphology False inflammation Inferred relationship Some 1
    Steatohepatitis caused by ingestible alcohol Associated morphology False inflammation 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 False inflammation Inferred relationship Some 1
    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 False inflammation Inferred relationship Some 2
    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 False inflammation Inferred relationship Some 1
    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 False inflammation Inferred relationship Some 1
    Molluscum contagiosum blepharoconjunctivitis Associated morphology False inflammation Inferred relationship Some 3
    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 False inflammation 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 inflammation Inferred relationship Some 1
    Rheumatoid arthritis of right knee (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Bilateral chronic tophaceous gout of hands Associated morphology False inflammation Inferred relationship Some 4
    Chronic tophaceous gout of bilateral elbows (disorder) Associated morphology False inflammation Inferred relationship Some 4
    Arthritis of acromioclavicular joint (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Eosinophilic inflammation Is a False inflammation Inferred relationship Some
    Manganese pneumonitis Associated morphology False inflammation Inferred relationship Some 1
    Acute berylliosis Associated morphology False inflammation Inferred relationship Some 1
    Cadmium pneumonitis Associated morphology False inflammation Inferred relationship Some 1
    Rheumatoid arthritis in remission (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Iritis of left eye due to diabetes mellitus Associated morphology False inflammation Inferred relationship Some 1
    Iritis of right eye due to diabetes mellitus (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Bilateral iritis due to diabetes mellitus Associated morphology False inflammation Inferred relationship Some 2
    Bilateral iritis due to diabetes mellitus Associated morphology False inflammation Inferred relationship Some 1
    Phlebitis of dorsal venous arch of foot (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Allergic contact dermatitis caused by iodophore (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Sepsis caused by virus (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Allergic contact dermatitis caused by povidone iodine (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Snow blindness Associated morphology False inflammation Inferred relationship Some 3
    Flash burn of eye Associated morphology False inflammation 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 False inflammation Inferred relationship Some 1
    Allergic contact dermatitis caused by iodine (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Blepharoconjunctivitis of left eye (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Blepharoconjunctivitis of left eye (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Blepharoconjunctivitis of right eye (disorder) Associated morphology False inflammation Inferred relationship Some 2
    Blepharoconjunctivitis of right eye (disorder) Associated morphology False inflammation Inferred relationship Some 1
    Blepharoconjunctivitis of bilateral eyes (disorder) Associated morphology False inflammation Inferred relationship Some 1

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