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
Familial obesity	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Constitutional obesity	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hyperplastic-hypertrophic obesity (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Lifelong obesity	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Buffalo obesity	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypertrophy of fat pad of knee	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	3
Adult-onset obesity (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
objektivt: overvægt	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Body mass index (kg/m²) equal to or greater than 40.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
objektivt: meget overvægtig	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	2
Drug-induced obesity	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Hyperplastic obesity (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Obese (finding)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Obesity (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Obesity by adipocyte growth pattern (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
adipositas specificeret iht. alder ved debut	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Obesity by contributing factors (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Obesity by fat distribution pattern (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Simple obesity (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
An X-linked retinal dystrophy characterized by choroideremia, causing in affected males progressive nyctalopia and eventual central blindness. Obesity, moderate intellectual disability and congenital mixed (sensorineural and conductive) deafness are also observed. Female carriers show typical retinal changes indicative of the choroideremia carrier state.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
A rare, X-linked syndromic intellectual disability disorder characterized by mild to moderate intellectual disability, obesity, hypogonadism, tapering fingers and microphallus with small or undescended testes, localized to Xp11.3-Xq23. Additional variable manifestations include alopecia, dental and eyesight anomalies, speech disabilities, and decreased body strength.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Wilson-Turner syndrome (WTS) is a very rare X-linked multisystem genetic disease characterized by intellectual disability, truncal obesity, gynecomastia, hypogonadism, dysmorphic facial features, and short stature.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
A rare form of syndromic obesity characterized by the association of congenital hydrocephalus, centripetal obesity, hypogonadism, intellectual deficit and short stature.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
A rare X-linked syndromic intellectual disability characterized by mild to profound intellectual disability, microcephaly, growth delay, and hypogenitalism. Obesity, early-onset diabetes and epilepsy are more variably present.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome is characterized by precocious obesity, congenital hypothyroidism, neonatal colitis, cardiac hypertrophy, craniosynostosis and developmental delay. It has been described in two brothers, one of whom died within the first month of life. The parents of the two children were nonconsanguineous and in good health, however, the pregnancies were complicated by a maternal HELLP syndrome (Haemolysis, Elevated Liver enzymes and Low Platelets). The mode of inheritance has not yet been clearly established.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	5
A rare genetic endocrine disease characterized by early onset of severe intractable diarrhea and intestinal malabsorption, followed by obesity and hormonal deficiencies due to insufficient activation of several prohormones, resulting in hypocortisolism, hypothyroidism, diabetes insipidus, hypogonadism, growth deficiency, and diabetes mellitus. Extent and age of onset of hormone deficiencies are variable between patients.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Overweight in adulthood with body mass index of 25 or more but less than 30 (finding)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Obesity caused by energy imbalance (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
MOMO syndrome is a very rare genetic overgrowth/obesity syndrome characterized by macrocephaly, obesity, mental (intellectual) disability and ocular abnormalities. Other frequent clinical signs include macrosomia, downslanting palpebral fissures, hypertelorism, broad nasal root, high and broad forehead and delay in bone maturation, in association with normal thyroid function and karyotype.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
A rare genetic syndromic intellectual disability characterized by language delay and mild to moderate intellectual disability associated with truncal obesity, congenital nonprogressive retinal dystrophy with poor night vision and reduced visual acuity, and micropenis in males. Cataracts may occur in the second or third decade of life.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early childhood, hyperphagia beginning in the first year of life and severe hyperinsulinemia, in the presence of preserved reproductive function.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Severe obesity complicating pregnancy	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Body mass index at or above 95th percentile as compared to children of the same age and sex	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Severe obesity	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
A rare genetic form of obesity characterised by morbid obesity, hypertension, type 2 diabetes mellitus and dyslipidaemia leading to early coronary disease, myocardial infarction and congestive heart failure. Intellectual disability and decreased sperm counts or azoospermia have also been reported.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
A rare genetic form of obesity characterised by severe early-onset obesity, hyperphagia, insulin resistance with hyperinsulinaemia, reduced adult final height, delayed speech and language development and a tendency for social isolation and aggressive behaviour.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
A rare genetic form of obesity with characteristics of severe early-onset obesity, hyperphagia and variable presence of cognitive impairment and behavioral disorder, including autistic spectrum behavior, impaired concentration and memory deficit. Some patients present with Prader-Willi-like features such as hypotonia, developmental delay, intellectual disability, short stature, hypopituitarism and dysmorphic facial features.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
A rare genetic non-syndromic obesity disease with characteristics of severe early-onset obesity associated with major hyperphagia and endocrine abnormalities resulting from leptin receptor deficiency. Caused by homozygous mutation in the gene encoding the leptin receptor (LEPR) on chromosome 1p31.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Body mass index percentile above the 85th and below the 95th percentile as compared to children of the same age and sex.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Maternal obesity complicating pregnancy, childbirth and the puerperium, antepartum	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Proopiomelanocortin deficiency causes severe obesity beginning at an early age. Affected individuals also have low levels of adrenocorticotropic hormone (ACTH) and tend to have red hair and pale skin.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Obesity in mother complicating childbirth (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
A rare group of multiple congenital anomalies/dysmorphic syndrome characterized by autism spectrum disorder, developmental delay, intellectual disability, hyperphagia/obesity, and short stature (clinical features overlapping with Prader-Willi syndrome). However, it is a clinically and genetically heterogenous group where patients may completely lack or manifests in minority some classical clinical features of Prader-Willi syndrome such as short stature, hypotonia, hypogonadism, hyperphagia and morbid obesity.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
Intellectual disability-seizures-macrocephaly-obesity syndrome is a rare syndromic obesity due to complex chromosomal rearrangement characterized by development delay and intellectual disability, childhood-onset obesity, seizures, poor coordination and broad-based gait, macrocephaly and mild dysmorphic features (such as narrow palpebral fissures, malar hypoplasia and thin upper lips), eczema, ocular abnormalities and a social personality.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome is a rare, syndromic intellectual disability primarily characterized by moderate to severe intellectual disability, true-to-relative microcephaly and brain abnormalities including a thin corpus callosum, cerebellar hypoplasia, cerebral white matter hypoplasia and multi-focal hyperintensity of cerebral white matter on MRI. Obesity and distinctive craniofacial dysmorphism (including brachycephaly, round face, straight eyebrows, synophrys, hypertelorism, epicanthus, wide and depressed nasal bridge, protruding ears with uplifted lobe, downslanting corners of the mouth) are additional features.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
A rare potentially life-threatening genetic endocrine disease characterised by childhood-onset hyperphagia and obesity, alveolar hypoventilation, dysautonomia (for example impaired gastrointestinal motility, abnormal cardiac rhythm, thermal dysregulation), hypothalamic dysfunction and neurobehavioural disorders. Central hypothyroidism, endocrine anomalies (for example glucocorticoid deficiency, puberty dysregulation), electrolyte imbalances (for example hypo/hypernatraemia, hypochloraemia), respiratory failure and late-onset neuroendocrine tumours may also be associated.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
A rare genetic syndromic intellectual disability disorder with characteristics of mild to profound intellectual disability, delayed speech, obesity, ocular anomalies (blepharophimosis, blepharoptosis, hyperopic astigmatism, decreased visual acuity, strabismus, abducens nerve palsy, and/or accommodative esotropia), and dermal manifestations, such as chronic atopic dermatitis. Associated craniofacial dysmorphism includes macrocephaly, maxillary hypoplasia, mandibular prognathism and crowding of teeth.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
Body mass index (kg/m²) from 30.00 to 34.99.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Body mass index (kg/m²) from 35.00 to 39.99.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Obese class III	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Hypertrophy of fat pad of right knee (disorder)	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	3
Hypertrophy of fat pad of left knee (disorder)	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	3
Obesity in adolescence (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Subcorneal pustular dermatosis with paraproteinemia (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Subcorneal pustular dermatosis with paraproteinemia (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
Episodic angioedema with eosinophilia (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Liver function test above reference range (finding)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Direct bilirubin above reference range	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Pulmonary arterial pressure increased (finding)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Eosinophilia due to infectious disease (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Fever caused by SARS-CoV-2	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Eosinophilic myositis (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Fasciitis with eosinophilia syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Eosinophilic colitis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Eosinophilic myopathy	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Eosinophilic fasciitis caused by L-tryptophan	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
A rare skeletal muscle disease with characteristics of eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue in the absence of an identifiable causative factor (for example parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties with walking, motor clumsiness, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia.	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	2
Eosinophilic ulcerative colitis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Carcinoid syndrome	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Carcinoid crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Diarrhea co-occurrent and due to carcinoid syndrome (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Viral load increased (finding)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Postmortem blood drug level increased	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Toxic goiter	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
diffus toksisk struma med eksoftalmi OG tyrotoksisk krise	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	4
Toxic uninodular goiter with thyrotoxic crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Toxic diffuse goiter with thyrotoxic crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Toxic diffuse goiter with pretibial myxedema	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Toxic multinodular goiter with thyrotoxic crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Exophthalmos due to toxic diffuse goiter	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	5
Toxic nodular goiter with thyrotoxic storm	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Graves' disease with acropachy AND with thyrotoxic crisis (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
Toxic diffuse goiter with acropachy	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Graves' disease with pretibial myxedema AND with thyrotoxic crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	5
Toxic diffuse goitre with no crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Toxic diffuse goitre with crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Toxic uninodular goiter with no crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Toxic multinodular goitre with no crisis	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Thyrotoxicosis due to Graves' disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Toxic diffuse goiter	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	1
Graves' disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Neonatal Graves' disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Toxic nodular goiter	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Toxic multinodular goiter	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Toxic uninodular goiter	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Graves' disease in remission (disorder)	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	4
Juvenile Graves' disease	Has interpretation	True	Above reference range (qualifier value)	Inferred relationship	Some	3
Dyshormonogenic goitre	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	1
Thyroglobulin synthesis defect	Has interpretation	False	Above reference range (qualifier value)	Inferred relationship	Some	3

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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)