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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
Glaucomatocyclitic crisis of right eye (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Glaucomatocyclitic crisis of right eye (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Glaucomatocyclitic crisis of left eye Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Glaucomatocyclitic crisis of left eye Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Glaucomatocyclitic crisis of bilateral eyes (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Glaucomatocyclitic crisis of bilateral eyes (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Glaucomatocyclitic crisis of bilateral eyes (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
Glaucomatocyclitic crisis of bilateral eyes (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 4
Infection caused by herpes zoster virus co-occurrent with human immunodeficiency virus infection (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of left lower leg Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of right lower leg Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of right thigh (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of left thigh (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of bilateral lower legs Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of bilateral lower legs Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Infective myositis of bilateral thighs (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of bilateral thighs (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Infective myositis of bilateral hands (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of bilateral hands (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Myositis of bilateral hands Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of right hand (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Myositis of left hand Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Myositis of right hand Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of left hand (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Myositis of bilateral hands Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Infective myositis of left upper arm (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of right upper arm Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of bilateral upper arms (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of bilateral upper arms (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Infective myositis of left shoulder (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of right shoulder (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of bilateral shoulders Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Infective myositis of bilateral shoulders Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Enteropathic arthritis of bilateral knee joints (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Enteropathic arthritis of bilateral knee joints (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Enteropathic arthritis of left knee joint (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Enteropathic arthritis of right knee joint (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Enteropathic arthritis of knee joint (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A spondyloarthritis associated predominately with inflammatory bowel diseases and less frequently with other intestinal disorders such Whipple disease, celiac disease and bowel-associated dermatitis-arthritis syndrome. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Arthritis temporally related to inflammatory bowel disease Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Bursitis of left elbow (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Bursitis of right elbow Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Acoustic neuritis of left ear due to infectious disease (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Right acoustic neuritis due to infectious disease Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Acoustic neuritis of bilateral ears due to infectious disease (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Acoustic neuritis of bilateral ears due to infectious disease (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Acoustic neuritis due to infectious disease (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare genetic gastroenterological disease characterized by infantile or childhood onset of severe gastrointestinal inflammation. Patients present with a variable phenotype including fever, diarrhea, failure to thrive, oral ulcers, fistulating perianal disease, strictures, granulomatous colitis, and recurrent bacterial and viral infections. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare autoimmune encephalitis involving the mesial temporal lobes and clinically characterised by subacute onset (rapid progression of less than three months) of short-term memory deficits, seizures or psychiatric symptoms, such as behavioural changes, anxiety, depression, and psychosis. Further diagnostic criteria are bilateral abnormalities restricted to the mesial temporal lobes in brain MRI, cerebrospinal fluid pleocytosis and/or epileptic or slow-wave activity involving the temporal lobes in EEG, and reasonable exclusion of alternative causes. Paraneoplastic or non-paraneoplastic antibodies against neuronal antigens may be found in serum and/or cerebrospinal fluid. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare autoimmune encephalitis involving the mesial temporal lobes and clinically characterised by subacute onset (rapid progression of less than three months) of short-term memory deficits, seizures or psychiatric symptoms, such as behavioural changes, anxiety, depression, and psychosis. Further diagnostic criteria are bilateral abnormalities restricted to the mesial temporal lobes in brain MRI, cerebrospinal fluid pleocytosis and/or epileptic or slow-wave activity involving the temporal lobes in EEG, and reasonable exclusion of alternative causes. Paraneoplastic or non-paraneoplastic antibodies against neuronal antigens may be found in serum and/or cerebrospinal fluid. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Endogenous lipoid pneumonitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Lupus pneumonitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Foreign body pneumonia Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Exogenous lipoid pneumonitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Traumatic pneumonitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Cholesterol pneumonitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Acute exogenous lipoid pneumonitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Lipoid pneumonitis due to vaping (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Bursitis of bilateral hands Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Lymphoid interstitial pneumonitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Arthritis of joint of bilateral wrist regions (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Arthritis of joint of bilateral wrist regions (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Arthritis of bilateral radiocarpal joints (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Arthritis of bilateral radiocarpal joints (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Arthritis of left radiocarpal joint Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Arthritis of right radiocarpal joint (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Chronic pneumonitis of infancy (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Drug-induced pneumonitis Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Pneumonia Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare, genetic, multisystemic, chronic autoimmune disease characterized by the presence of systemic lupus erythematosus symptoms in two or more members of a single family. Patients present a wide spectrum of clinical manifestations, including cutaneous (malar rash, photosensitivity), ocular (keratoconjunctivitis sicca, retinopathy), gastrointestinal (oral ulceration, abdominal pain), cardiac (atherosclerosis, chest pain), pulmonary (serositis, pleurisy), musculoskeletal (arthralgia, myalgia), renal (nephritis, hematuria), obstetrical (increased spontaneous abortions, neonatal lupus), constitutional (fatigue, loss of appetite) and neuropsychiatric (mood and cognitive disorders) involvement, among others. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Mendelian susceptibility to mycobacterial diseases (MSMD) due to complete ISG15 deficiency is a genetic variant of MSMD characterized by Bacille Calmette-Guérin (BCG) infections. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare genetic cerebral small vessel disease characterized by progressive loss of visual acuity due to retinal vasculopathy, in combination with more variable neurological signs and symptoms including stroke, cognitive decline, migraine-like headaches, and seizures, among others, typically beginning in middle age. Psychiatric features such as depression and anxiety may also occur. Systemic vascular involvement with Raynaud phenomenon, micronodular liver cirrhosis, and glomerular kidney dysfunction is present in a subset of patients. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 6
A rare monogenic form of cutaneous lupus erythematosus characterised by infantile or childhood onset of cold-induced erythematous papules or plaques predominantly on the fingers, toes, nose, cheeks, and ears. Recurrent ulceration of the lesions may lead to necrotic tissue destruction and mutilation. Patients may experience ischaemia of the affected acral regions. Histological findings include cutaneous perivascular inflammatory infiltrates with deposits of immunoglobulins or complement. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 4
Spondyloenchondrodysplasia Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
Singleton-Merten syndrome Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
Trichohepatoenteric syndrome Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
Spondyloenchondrodysplasia with immune dysregulation Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
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 2
X-linked reticulate pigmentary disorder is an extremely rare skin disease described in only four families to date and characterized in males by diffuse reticulate brown hyperpigmented skin lesions developing in early childhood and a variety of systemic manifestations (recurrent pneumonia, corneal opacification, gastrointestinal inflammation, urethral stricture, failure to thrive, hypohidrosis, digital clubbing, and unruly hair and flared eyebrows), while in females, there is only cutaneous involvement with the development in early childhood of localized brown hyperpigmented skin lesions following the lines of Blaschko. This disease was first considered as a cutaneous amyloidosis, but amyloid deposits are an inconstant feature. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
A rare genetic systemic or rheumatologic disease characterized by interstitial lung disease (often with pulmonary hemorrhage) and inflammatory arthritis, associated with high-titer autoantibodies (including anti-nuclear and anti-neutrophil cytoplasmic antibodies, and rheumatoid factor). Patients present from infancy to adolescence with tachypnea, cough, hemoptysis, and/or joint pain. Some patients may also develop glomerular disease. Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 4
Acute endogenous lipoid pneumonitis (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 3
Pneumonia caused by Mycoplasma pneumoniae Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
A rare hypersensitivity reaction with characteristics of the rapid development of numerous, nonfollicular, sterile, pinhead-sized pustules on an erythematous base, predominantly occurring on the trunk, intertriginous and flexural areas, with rare, mostly oral, mucosal involvement. Fever, peripheral blood leukocytosis, and mild eosinophilia are accompanying features. Systemic involvement, with hepatic, renal or pulmonary dysfunction, occasionally occurs. Onset usually occurs 1-12 days after administration of the causal medication and is most frequently associated with beta‐lactam antibiotics, macrolides (including pristinamycin and clindamycin), diltiazem, terbinafine, (hydroxy‐)chloroquine but many other medications have also been implicated. Histology reveals spongiform, subcorneal and/or intraepidermal, pustules but this pattern is not specific (same in pustular psoriasis). Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Periodic fever, immunodeficiency, thrombocytopenia syndrome (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Meningitis caused by Citrobacter (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Sepsis due to infection caused by Citrobacter (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Arthritis of joint of hand (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Arthritis of joint of foot (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Arthritis of sacroiliac joint Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Inflammation of right sacroiliac joint (finding) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Inflammation of left sacroiliac joint (finding) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Inflammation of bilateral sacroiliac joints (finding) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Inflammation of bilateral sacroiliac joints (finding) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 2
Arthritis of shoulder region joint Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Neuritis of left ulnar nerve (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Neuritis of right ulnar nerve (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Conjunctival blebitis of left eye following glaucoma surgery Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Conjunctival blebitis of right eye following glaucoma surgery (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Conjunctival blebitis of bilateral eyes following glaucoma surgery (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Uveitis-glaucoma-hyphema syndrome of left eye Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1
Uveitis-glaucoma-hyphema syndrome of right eye (disorder) Associated morphology True Inflammatory morphology (morphologic abnormality) Inferred relationship Some 1

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