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281302008: Above reference range (qualifier value)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
419285019 Above reference range en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
674822016 Above reference range (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Above reference range Is a Reference range comments false Inferred relationship Some
Above reference range Is a Outside reference range (qualifier value) true Inferred relationship Some
Above reference range Is a Increased true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Alpha heavy chain disease (clinical) Has interpretation True Above reference range Inferred relationship Some 2
Stress polycythemia Has interpretation True Above reference range Inferred relationship Some 1
Polycythemia due to donor twin transfusion Has interpretation True Above reference range Inferred relationship Some 1
Idiopathic erythrocytosis Has interpretation True Above reference range Inferred relationship Some 1
Biclonal gammopathy Has interpretation True Above reference range Inferred relationship Some 3
Hemoglobinopathy with erythrocytosis Has interpretation True Above reference range Inferred relationship Some 1
Familial erythrocytosis Has interpretation True Above reference range Inferred relationship Some 1
TEMPI syndrome is a rare multi-systemic disease characterized by the presence of Telangiectasias, Erythrocytosis with elevated erythropoietin levels, Monoclonal gammopathy, Perinephric-fluid collections, and Intrapulmonary shunting. Has interpretation True Above reference range Inferred relationship Some 3
Macroglobulinemia Has interpretation True Above reference range Inferred relationship Some 2
Waldenström macroglobulinaemia Has interpretation True Above reference range Inferred relationship Some 2
Erythrocytosis due to autotransfusion Has interpretation True Above reference range Inferred relationship Some 1
Secondary polycythaemia Has interpretation True Above reference range Inferred relationship Some 1
Monoclonal paraproteinemia Has interpretation False Above reference range Inferred relationship Some 3
Polycythaemia due to cyanotic heart disease Has interpretation True Above reference range Inferred relationship Some 1
Polycythaemia due to cyanotic respiratory disease Has interpretation True Above reference range Inferred relationship Some 1
Triclonal gammopathy Has interpretation True Above reference range Inferred relationship Some 3
POEMS syndrome Has interpretation True Above reference range Inferred relationship Some 3
Erythrocytosis due to alveolar hypoventilation Has interpretation True Above reference range Inferred relationship Some 1
Amyloid light-chain nephropathy (disorder) Has interpretation True Above reference range Inferred relationship Some 4
Erythrocytosis due to hydronephrosis Has interpretation True Above reference range Inferred relationship Some 1
Monoclonal gammopathy (clinical) Has interpretation True Above reference range Inferred relationship Some 2
Mixed cryoimmunoglobulinemia with monoclonal component Has interpretation True Above reference range Inferred relationship Some 3
Sporadic primary amyloidosis Has interpretation True Above reference range Inferred relationship Some 3
Erythrocytosis due to tissue hypoxemia Has interpretation True Above reference range Inferred relationship Some 1
Polycythemia neonatorum following blood transfusion (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Erythrocytosis due to uterine myoma Has interpretation True Above reference range Inferred relationship Some 1
AL amyloidosis Has interpretation True Above reference range Inferred relationship Some 2
Light chain deposition disease (disorder) Has interpretation True Above reference range Inferred relationship Some 2
Benign paraproteinaemia Has interpretation True Above reference range Inferred relationship Some 2
Epsilon heavy chain disease Has interpretation False Above reference range Inferred relationship Some 3
Monoclonal gammopathy of uncertain significance Has interpretation True Above reference range Inferred relationship Some 2
Gamma heavy chain disease (clinical) Has interpretation True Above reference range Inferred relationship Some 3
Kappa light chain disease Has interpretation True Above reference range Inferred relationship Some 2
Delta heavy chain disease Has interpretation False Above reference range Inferred relationship Some 3
Lambda light chain disease Has interpretation True Above reference range Inferred relationship Some 2
Heavy chain disease Has interpretation True Above reference range Inferred relationship Some 2
TEMPI syndrome is a rare multi-systemic disease characterized by the presence of Telangiectasias, Erythrocytosis with elevated erythropoietin levels, Monoclonal gammopathy, Perinephric-fluid collections, and Intrapulmonary shunting. Has interpretation True Above reference range Inferred relationship Some 2
IgA monoclonal gammopathy of uncertain significance Has interpretation True Above reference range Inferred relationship Some 3
IgG monoclonal gammopathy of uncertain significance Has interpretation True Above reference range Inferred relationship Some 3
Light chain monoclonal gammopathy of uncertain significance Has interpretation True Above reference range Inferred relationship Some 3
Idiopathic hypercalcaemia Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia due to immobilization Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia due to sarcoidosis Has interpretation True Above reference range Inferred relationship Some 1
Humoral hypercalcemia of malignancy Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia due to tuberculosis (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Milk alkali syndrome Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia due to hyperthyroidism Has interpretation True Above reference range Inferred relationship Some 1
Infantile hypercalcemia Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia due to granulomatous disease Has interpretation True Above reference range Inferred relationship Some 1
Idiopathic infantile hypercalcaemia - mild form Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia due to hypervitaminosis D (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Idiopathic hypercalcemia of infancy Has interpretation True Above reference range Inferred relationship Some 1
Myopathy co-occurrent and due to hypercalcemia (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia associated with chronic dialysis Has interpretation True Above reference range Inferred relationship Some 1
Chronic milk alkali syndrome Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia caused by a drug (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcemia caused by thiazide AND vitamin A Has interpretation False Above reference range Inferred relationship Some 1
Secondary hypercalcaemia Has interpretation True Above reference range Inferred relationship Some 1
Nutritional disorder due to calcium-phosphorus imbalance Has interpretation True Above reference range Inferred relationship Some 1
Hypercalcaemia caused by lithium Has interpretation True Above reference range Inferred relationship Some 1
Subacute milk alkali syndrome Has interpretation True Above reference range Inferred relationship Some 1
Familial hypocalciuric hypercalcaemia Has interpretation True Above reference range Inferred relationship Some 1
Acquired hypocalciuric hypercalcaemia Has interpretation True Above reference range Inferred relationship Some 1
Hypocalciuric hypercalcemia Has interpretation True Above reference range Inferred relationship Some 1
Acute milk alkali syndrome Has interpretation True Above reference range Inferred relationship Some 1
Severe idiopathic hypercalcemia of infancy (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Hyperfibrinogenemia (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Hyperviscosity syndrome (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Hereditary hyperfibrinogenemia (disorder) Has interpretation True Above reference range Inferred relationship Some 1
Chuvash erythrocytosis is a rare, genetic, congenital secondary polycythemia disorder characterized by increased hemoglobin, hematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnea and/or plethora. Patients present an increased risk of hemorrhage, thrombosis and early death. Has interpretation True Above reference range Inferred relationship Some 1
Infection caused by Borrelia miyamotoi Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever Has interpretation False Above reference range Inferred relationship Some 1
Tick-borne relapsing fever Has interpretation True Above reference range Inferred relationship Some 1
Acute gout Has interpretation False Above reference range Inferred relationship Some 1
Testosterone level above reference range Has interpretation False Above reference range Inferred relationship Some 2
Hypermobility of coccyx Has interpretation True Above reference range Inferred relationship Some 1
Relapsing fever of Southern United States, Mexico, Central AND/OR South America Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever of Iran AND/OR Central Asia Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever caused by Borrelia recurrentis Has interpretation True Above reference range Inferred relationship Some 2
Relapsing fever of Western United States Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever of Iberian Peninsula AND/OR Northwest Africa Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever of Western North America Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever of Asia AND/OR Africa Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever of Central AND/OR South Africa Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever of Central AND/OR South America Has interpretation False Above reference range Inferred relationship Some 2
Relapsing fever of the Caucasus Has interpretation False Above reference range Inferred relationship Some 2
Hyperbiliverdinemia is a rare, genetic hepatic disease characterized by the presence of green coloration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. Has interpretation True Above reference range Inferred relationship Some 1
A rare, genetic, phosphocalcic metabolism disorder characterized by early-onset hypercalcemia, hypophosphatemia, hypercalciuria, decreased intact parathyroid hormone serum levels and medullary nephrocalcinosis, typically manifesting with failure to thrive, hypotonia, vomiting, constipation and/or polyuria. Has interpretation True Above reference range Inferred relationship Some 1
Thrombocythemia with distal limb defects is a rare, genetic syndrome with limb reduction defects characterized by thrombocytosis, unilateral transverse limb defects (ranging from absence of phalanges to absence of hand or forearm) and splenomegaly. Has interpretation True Above reference range Inferred relationship Some 1
Hypermobility of thoracic spine (finding) Has interpretation True Above reference range Inferred relationship Some 1
Transient infantile hypertriglyceridemia and hepatosteatosis is a rare, genetic, hepatic disease characterized by massive hepatomegaly, moderate to severe, transient hypertriglyceridemia and hepatic steatosis (followed by fibrosis), manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fatty liver. Reduction or normalization of triglyceride serum levels occurs with advancing age. Has interpretation True Above reference range Inferred relationship Some 1
A rare sterol metabolism disorder characterized by increased LDL cholesterol serum levels (which are resistant to treatment with 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors), hypertriglyceridemia, and decreased rate of bile acid excretion, resulting from cholesterol 7alpha-hydroxylase deficiency. Premature gallstone disease and/or premature coronary and peripheral vascular disease are frequently associated. Has interpretation True Above reference range Inferred relationship Some 1
Gouty arthritis of right ankle (disorder) Has interpretation False Above reference range Inferred relationship Some 1
Gouty arthritis of left ankle Has interpretation False Above reference range Inferred relationship Some 1
Gouty arthritis of left hand Has interpretation False Above reference range Inferred relationship Some 2
Gouty arthritis of right hand (disorder) Has interpretation False Above reference range Inferred relationship Some 1
Gouty arthritis of left knee (disorder) Has interpretation False Above reference range Inferred relationship Some 1
Gouty arthritis of right knee (disorder) Has interpretation False Above reference range Inferred relationship Some 1
A rare genetic epidermal disorder characterized by congenital erythroderma with severe psoriasiform dermatitis, ichthyosis, severe palmoplantar keratoderma, yellow keratosis on the hands and feet, elevated immunoglobulin E, multiple food allergies, and metabolic wasting. Other variable features may include hypotrichosis, nail dystrophy, recurrent infections, mild global developmental delay, eosinophilia, nystagmus, growth impairment and cardiac defects. Has interpretation True Above reference range Inferred relationship Some 2
Gouty arthritis of left elbow Has interpretation False Above reference range Inferred relationship Some 1

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