900000000000508004: Great Britain English language reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Language type reference set (foundation metadata concept)\English [International Organization for Standardization 639-1 code en] language reference set (foundation metadata concept)\GB English

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
GB English	Is a	English [International Organization for Standardization 639-1 code en] language reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	acceptabilityId
9q31.1q31.3 microdeletion syndrome	Preferred (foundation metadata concept)
9q31.1q31.3 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
9q33.3q34.11 microdeletion syndrome	Preferred (foundation metadata concept)
9q33.3q34.11 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
9q34 deletion syndrome	Preferred (foundation metadata concept)
9q34 deletion syndrome (disorder)	Preferred (foundation metadata concept)
9th floor	Acceptable (foundation metadata concept)
9x/day	Acceptable (foundation metadata concept)
:: Gamma heavy chain disease	Acceptable (foundation metadata concept)
<	Preferred (foundation metadata concept)
< 4 mitoses/high power field	Preferred (foundation metadata concept)
< 4 mitoses/high power field (finding)	Preferred (foundation metadata concept)
<1.5 hours sent off: [DS4] or [DS1500]	Preferred (foundation metadata concept)
<1.5 hours sent off: [DS4] or [DS1500] (finding)	Preferred (foundation metadata concept)
<2 fingers	Preferred (foundation metadata concept)
<2 fingers (qualifier value)	Preferred (foundation metadata concept)
<3	Preferred (foundation metadata concept)
<3 (qualifier value)	Preferred (foundation metadata concept)
<35 degrees C	Acceptable (foundation metadata concept)
<90	Preferred (foundation metadata concept)
<90 (qualifier value)	Preferred (foundation metadata concept)
<90 degrees	Preferred (foundation metadata concept)
<90 degrees (qualifier value)	Preferred (foundation metadata concept)
<=	Preferred (foundation metadata concept)
=	Preferred (foundation metadata concept)
>	Preferred (foundation metadata concept)
> 4 mitoses/high power field	Acceptable (foundation metadata concept)
>10 mitoses per 10 HPF (score = 3)	Acceptable (foundation metadata concept)
>2 fingers	Preferred (foundation metadata concept)
>2 fingers (qualifier value)	Preferred (foundation metadata concept)
>2.5 hours sent off: [DS4] or [DS1500]	Preferred (foundation metadata concept)
>2.5 hours sent off: [DS4] or [DS1500] (finding)	Preferred (foundation metadata concept)
>20 mitoses per 10 HPF (score = 3)	Acceptable (foundation metadata concept)
>35 degrees C	Acceptable (foundation metadata concept)
>4 cusps	Preferred (foundation metadata concept)
>4 cusps (qualifier value)	Preferred (foundation metadata concept)
>5	Preferred (foundation metadata concept)
>5 (qualifier value)	Preferred (foundation metadata concept)
>50 degrees C	Acceptable (foundation metadata concept)
>90	Preferred (foundation metadata concept)
>90 (qualifier value)	Preferred (foundation metadata concept)
>90 degrees	Preferred (foundation metadata concept)
>90 degrees (qualifier value)	Preferred (foundation metadata concept)
>97	Preferred (foundation metadata concept)
>97 (qualifier value)	Preferred (foundation metadata concept)
>=	Preferred (foundation metadata concept)
? child now: [EC69] or [EC60] from FPC] or [EC69 from HB]	Preferred (foundation metadata concept)
? child now: [EC69] or [EC60] from FPC] or [EC69 from HB]	Preferred (foundation metadata concept)
? child now: [EC69] or [EC60] from FPC] or [EC69 from HB] (finding)	Preferred (foundation metadata concept)
? child now: [EC69] or [EC60] from FPC] or [EC69 from HB] (finding)	Preferred (foundation metadata concept)
? patient now: [FP69 from FPC] or [GP69 from HB]	Preferred (foundation metadata concept)
? patient now: [FP69 from FPC] or [GP69 from HB]	Preferred (foundation metadata concept)
? patient now: [FP69 from FPC] or [GP69 from HB] (finding)	Preferred (foundation metadata concept)
? patient now: [FP69 from FPC] or [GP69 from HB] (finding)	Preferred (foundation metadata concept)
A	Preferred (foundation metadata concept)
A	Preferred (foundation metadata concept)
A & E - Accident and Emergency Department	Acceptable (foundation metadata concept)
A & E service	Acceptable (foundation metadata concept)
A (tumor staging)	Preferred (foundation metadata concept)
A - alphalipoproteinaemia neuropathy	Acceptable (foundation metadata concept)
A - ampere	Preferred (foundation metadata concept)
A 102	Preferred (foundation metadata concept)
A 102 (qualifier value)	Preferred (foundation metadata concept)
A Noonan-related syndrome with characteristics of facial anomalies suggestive of Noonan syndrome, a distinctive hair anomaly described as loose anagen hair syndrome, frequent congenital heart defects, distinctive skin features with darkly pigmented skin, keratosis pilaris, eczema or occasional neonatal ichthyosis and short stature, often associated with a growth hormone deficiency and psychomotor delay. There is evidence that this syndrome is caused by heterozygous mutation in the SHOC2 gene on chromosome 10q25.	Preferred (foundation metadata concept)
A Wernicke-like encephalopathy with characteristics of seizures responsive to high doses of thiamine. Two cases have been described so far. Clinical features include epilepsy, nystagmus, ophthalmoplegia and ataxia. The disease results from mutations in the SLC19A3 gene, encoding a thiamine transporter. Transmission is autosomal recessive.	Preferred (foundation metadata concept)
A Z-shaped cut in the first metatarsal in order to separate the head of the plantar half of the shaft from the rest of the bone. This allows the head-shaft complex to be translated and rotated in order to achieve correction of the deformity while maintaining articular congruity.	Preferred (foundation metadata concept)
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalised areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense.	Preferred (foundation metadata concept)
A alphanumeric labels	Preferred (foundation metadata concept)
A alphanumeric labels (qualifier value)	Preferred (foundation metadata concept)
A antigen	Acceptable (foundation metadata concept)
A band	Preferred (foundation metadata concept)
A band (cell structure)	Preferred (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex characterised by generalised blistering associated with muscular dystrophy. Onset of blistering is usually as early as birth, muscular dystrophy manifests between infancy and adulthood. Blisters are often haemorrhagic and heal with mild atrophic scarring and rare milia formation. Associated findings comprise markedly dystrophic nails, and focal keratoderma of the palms and soles. Extracutaneous involvement is usually present. Caused by mutations in the PLEC gene (8q24) encoding plectin. Plectin deficiency can be demonstrated in skin and muscle by analysis with specific antibodies. Transmission is autosomal recessive.	Preferred (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex characterised by generalised or, less frequently, localised acral blistering. 19 cases have been reported to date. Onset of the disease is usually at birth. Milia are rare but atrophic scarring and dystrophic nails usually occur, along with focal keratoderma (palms and soles) and rarely ichthyotic plaques. Extracutaneous involvement is common, including anaemia, growth retardation, oral cavity abnormalities (blisters and erosions, and caries) and constipation. Due to mutations in the KRT14 gene (17q12-q21), encoding keratin 14. Transmission is autosomal recessive.	Preferred (foundation metadata concept)
A benign epithelial ovarian tumour characterised by a usually unilateral, cystic, unilocular or multilocular lesion with a thin wall or septa and no intracystic solid portion on imaging. It often presents with abdominal pain or an asymptomatic abdominal mass and can be associated with ovarian torsion or malignant transformation.	Preferred (foundation metadata concept)
A benign form of holoprosencephaly characterised by midline defects without the typical HPE defect in brain cleavage and which can variably manifest with microcephaly, hypotelorism, midline cleft lip and/or flat nose, choanal stenosis, pyriform sinus stenosis, coloboma as well as a single median maxillary incisor.	Preferred (foundation metadata concept)
A benign natural killer (NK) cell lymphoproliferative disease with characteristics of minor abdominal symptoms (abdominal pain, diverticulosis, constipation and reflux) due to NK cell-derived lesions in the mucosal layer of the gastrointestinal tract and often mistaken for NK or T-cell lymphoma.	Preferred (foundation metadata concept)
A benign pituitary gland neoplasm occurring separately from and without involvement of the sella turcica.	Preferred (foundation metadata concept)
A benign proliferation of pigment cells of the oral mucosa producing brown or bluish dome-shaped or sessile mass, usually with a smooth surface.	Preferred (foundation metadata concept)
A benign tumour invasive into adjacent structures.	Preferred (foundation metadata concept)
A benign vasoproliferative lesion in which lymph node sinuses become converted to anastomosing endothelial-lined channels.	Preferred (foundation metadata concept)
A bilateral tonic-clonic epileptic seizure of more than 5 minutes duration. The seizure may be focal, generalised or unknown onset.	Preferred (foundation metadata concept)
A biofield therapy that relies upon a belief in an invisible energy that may be transmitted from healer to patient through intention.	Preferred (foundation metadata concept)
A bleeding disorder associated with a decreased ability to form blood clots resulting in increased risk of epistaxis, heavy or prolonged bleeding following minor injury or surgery, ecchymosis and menorrhagia. The disease can be caused by mutations in the GP6 gene, leading to the production of no glycoprotein VI (GPVI) protein, an abnormally short, nonfunctional GPVI protein; or a protein that is less able to bind to collagen. Without GPVI binding to collagen, platelets cannot come together efficiently to form a clot. The disease may also be acquired rather than inherited and such cases are associated with autoimmune disorders such as systemic lupus erythematosus (SLE).	Preferred (foundation metadata concept)
A bleeding disorder with characteristics of mild to moderate mucocutaneous bleeding, which becomes more pronounced during pregnancy or following ingestion of drugs that have anti-platelet activity. This disease is due to hyperresponsive platelets, resulting in thrombocytopenia.	Preferred (foundation metadata concept)
A blood group typing	Acceptable (foundation metadata concept)
A blood pressure observable where placement of several pneumatic cuffs on the limbs determine the pressure at multiple locations in efforts to localize arterial occlusions	Preferred (foundation metadata concept)
A blood pressure that refers to the average over a cardiac cycle	Preferred (foundation metadata concept)
A blood pressure which is observed by a non-invasive procedure, one that does not involve entry into a patient such using as a pressure cuff	Preferred (foundation metadata concept)
A blood pressure which is observed by an invasive procedure, one that involves entry into a patient such as inserting a cannula needle in an artery	Preferred (foundation metadata concept)
A board-certified physician who has finished residency training and is pursuing subspecialisation within an area of interest.	Preferred (foundation metadata concept)
A body cavity route of administration by entry into the peritoneum.	Preferred (foundation metadata concept)
A body cavity route that begins within the bladder cavity.	Preferred (foundation metadata concept)
A body cavity route that begins within the uterine cavity.	Preferred (foundation metadata concept)
A brain malformation due to abnormal neuronal migration, in which a subset of neurons fails to migrate into the developing cerebral cortex and remains as nodules that line the ventricular surface. Classical periventricular nodular heterotopia is a rare X-linked dominant disorder far more frequent in females who present normal intelligence to borderline intellectual deficit, epilepsy of variable severity and extra-central nervous system signs, especially cardiovascular defects or coagulopathy. The disorder is generally associated with prenatal lethality in males.	Preferred (foundation metadata concept)
A broad spectrum of other macroreentrant tachycardias in which the wave front does not travel around the tricuspid annulus. Atypical atrial flutter originates from the left atrium or areas in the right atrium (such as surgical scars) and has a variable appearance on ECG in regards to the flutter waves.	Preferred (foundation metadata concept)
A broad term that encompasses several types of imaging studies that use ionising radiation for visualisation of internal parts of the body using X-ray techniques, for example computed tomography.	Preferred (foundation metadata concept)
A broader region is formed by the union of the posterior and lateral chest walls.	Preferred (foundation metadata concept)
A bungee cord is a long nylon-cased rubber band with hooks at each end that is used for securing luggage and other items.	Preferred (foundation metadata concept)
A calculation using actual body weight divided by usual body weight and expressed as a percentage.	Preferred (foundation metadata concept)
A calorie-controlled, prepackaged product in the form of a bar or beverage that replaces a regular meal.	Preferred (foundation metadata concept)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001112010	Great Britain English language reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001113017	GB English	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001114011	Great Britain English language reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)