281302008: Above reference range (qualifier value)

SNOMED CT Concept\Qualifier value\...

\Descriptor (qualifier value)\Increased\Above reference range (qualifier value)

\Finding value (qualifier value)\Interpretation value\Reference range interpretation value\Outside reference range (qualifier value)\Above reference range (qualifier value)
\Finding value (qualifier value)\Finding status values (qualifier value)\Change values\Changed status\Increased\Above reference range (qualifier value)
\Finding value (qualifier value)\Degree findings\Increased\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

3824241000005112 over referenceinterval da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Above reference range (qualifier value)	Is a	Reference range comments	false	Inferred relationship	Some
Above reference range (qualifier value)	Is a	Outside reference range (qualifier value)	true	Inferred relationship	Some
Above reference range (qualifier value)	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 (qualifier value)	Inferred relationship	Some	2
Stress polycythemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Polycythemia due to donor twin transfusion	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Idiopathic erythrocytosis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Biclonal gammopathy	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Hemoglobinopathy with erythrocytosis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Familial erythrocytosis	Has interpretation	True	Above reference range (qualifier value)	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 (qualifier value)	Inferred relationship	Some	3
Macroglobulinaemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Waldenström macroglobulinaemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Erythrocytosis due to autotransfusion	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Secondary polycythemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
monoklonal paraproteinæmi	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	3
Polycythemia due to cyanotic heart disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Polycythemia due to cyanotic respiratory disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Triclonal gammopathy	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
POEMS syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Erythrocytosis due to alveolar hypoventilation	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Amyloid light-chain nephropathy (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
Erythrocytosis due to hydronephrosis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Monoclonal gammopathy (clinical)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Mixed cryoimmunoglobulinemia with monoclonal component	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Sporadic primary amyloidosis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Erythrocytosis due to tissue hypoxemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Polycythemia neonatorum following blood transfusion (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Erythrocytosis due to uterine myoma	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
AL amyloidosis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Light chain deposition disease (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Benign paraproteinaemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
epsilon-heavy chain disease	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	3
Monoclonal gammopathy of uncertain significance	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Gamma heavy chain disease (clinical)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Kappa light chain disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
delta-heavy chain disease	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	3
Lambda light chain disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Heavy chain disease (disorder)	Has interpretation	True	Above reference range (qualifier value)	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 (qualifier value)	Inferred relationship	Some	2
IgA monoclonal gammopathy of uncertain significance	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
IgG monoclonal gammopathy of uncertain significance	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Light chain monoclonal gammopathy of uncertain significance	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Idiopathic hypercalcemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia due to immobilization	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia due to sarcoidosis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Humoural hypercalcaemia of malignancy	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia due to tuberculosis (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Milk alkali syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia due to hyperthyroidism	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Infantile hypercalcemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia due to granulomatous disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Idiopathic infantile hypercalcaemia - mild form	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia due to hypervitaminosis D (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Idiopathic hypercalcemia of infancy	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Myopathy co-occurrent and due to hypercalcemia (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia associated with chronic dialysis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Chronic milk alkali syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcemia caused by a drug (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
hyperkalcæmi forårsaget af thiazid OG A-vitamin	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Secondary hypercalcaemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Nutritional disorder due to calcium-phosphorus imbalance	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypercalcaemia caused by lithium	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Subacute milk alkali syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Familial hypocalciuric hypercalcaemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Acquired hypocalciuric hypercalcaemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypocalciuric hypercalcemia	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Acute milk alkali syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Severe idiopathic hypercalcemia of infancy (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hyperfibrinogenemia (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hyperviscosity syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hereditary hyperfibrinogenemia (disorder)	Has interpretation	True	Above reference range (qualifier value)	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 (qualifier value)	Inferred relationship	Some	1
Infection caused by Borrelia miyamotoi	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Tick-borne relapsing fever	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Acute gout	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Testosterone level above reference range	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
Hypermobility of coccyx	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
febris recurrens fra det sydlige USA, Mexico, Central- OG/ELLER Sydamerika	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens fra Iran OG/ELLER Centralasien	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
Relapsing fever caused by Borrelia recurrentis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens fra det vestlige USA	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens fra Den iberiske Halvø OG/ELLER Nordvestafrika	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens fra det vestlige Nordamerika	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens fra Asien OG/ELLER Afrika	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens fra Central- OG/ELLER Sydafrika	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens fra Central- OG/ELLER Sydamerika	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
febris recurrens fra Kaukasus	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
A rare genetic hepatic disease characterised by the presence of green colouration 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. Can be caused by heterozygous or homozygous mutation in the gene encoding bilirubin reductase-alpha (BLVRA) on chromosome 7p13.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
A rare genetic phospho-calcic metabolism disorder characterised by early-onset hypercalcaemia, hypophosphataemia, 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 (qualifier value)	Inferred relationship	Some	1
A rare genetic syndrome with limb reduction defects with characteristics of thrombocytosis, unilateral transverse limb defects (ranging from absence of phalanges to absence of hand or forearm) and splenomegaly.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypermobility of thoracic spine (finding)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
A rare genetic hepatic disease characterised by massive hepatomegaly, moderate to severe transient hypertriglyceridaemia and hepatic steatosis (followed by fibrosis) manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fatty liver. Reduction or normalisation of triglyceride serum levels occurs with advancing age. Caused by homozygous or compound heterozygous mutation in the GPD1 gene on chromosome 12q13.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
A rare genetic 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 (qualifier value)	Inferred relationship	Some	1
Gouty arthritis of right ankle (disorder)	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Gouty arthritis of left ankle	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Gouty arthritis of left hand	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
Gouty arthritis of right hand (disorder)	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Gouty arthritis of left knee (disorder)	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Gouty arthritis of right knee (disorder)	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
A rare genetic epidermal disorder with characteristics of 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 (qualifier value)	Inferred relationship	Some	2
Gouty arthritis of left elbow	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1

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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
3824241000005112	over referenceinterval	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)