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
A route that begins anywhere in the digestive tract extending from the mouth through the rectum.	Preferred (foundation metadata concept)
A route that begins around a nerve or nerves.	Preferred (foundation metadata concept)
A route that begins around a tendon.	Preferred (foundation metadata concept)
A route that begins beneath a tendon.	Preferred (foundation metadata concept)
A route that begins beneath the mucous membrane.	Preferred (foundation metadata concept)
A route that begins in subcutaneous tissue.	Preferred (foundation metadata concept)
A route that begins in the cervix uteri.	Preferred (foundation metadata concept)
A route that begins in the eye region.	Preferred (foundation metadata concept)
A route that begins in the regional surrounding a tumour.	Preferred (foundation metadata concept)
A route that begins in the vagina.	Preferred (foundation metadata concept)
A route that begins inside of the trachea specifically, and does not include the potential administration directly to pulmonary locations.	Preferred (foundation metadata concept)
A route that begins next to one or more vertebra.	Preferred (foundation metadata concept)
A route that begins next to the uterine cervix.	Preferred (foundation metadata concept)
A route that begins on the eyeball or conjunctiva.	Preferred (foundation metadata concept)
A route that begins on the surface of a localised lesion.	Preferred (foundation metadata concept)
A route that begins on the surface of mucosal tissue and has the propensity for systemic absorption via the submucosa.	Preferred (foundation metadata concept)
A route that begins on the surface of the body.	Preferred (foundation metadata concept)
A route that begins on, in or by way of the ear.	Preferred (foundation metadata concept)
A route that begins through a fistula.	Preferred (foundation metadata concept)
A route that begins through a surgical drain.	Preferred (foundation metadata concept)
A route that begins through a surgically created opening into the urinary tract.	Preferred (foundation metadata concept)
A route that begins through the cervix.	Preferred (foundation metadata concept)
A route that begins with diffusion or accumulation in a tissue or cells.	Preferred (foundation metadata concept)
A route that begins with the vascular system.	Preferred (foundation metadata concept)
A route that begins within a bursa.	Preferred (foundation metadata concept)
A route that begins within a gland.	Preferred (foundation metadata concept)
A route that begins within a joint.	Preferred (foundation metadata concept)
A route that begins within a localised lesion.	Preferred (foundation metadata concept)
A route that begins within a muscle.	Preferred (foundation metadata concept)
A route that begins within a non-pathologic hollow cavity, such as that of the abdominal cavity or uterus.	Preferred (foundation metadata concept)
A route that begins within a pathologic cavity.	Preferred (foundation metadata concept)
A route that begins within a surgical cavity.	Preferred (foundation metadata concept)
A route that begins within a tendon.	Preferred (foundation metadata concept)
A route that begins within a tumour.	Preferred (foundation metadata concept)
A route that begins within a ureter.	Preferred (foundation metadata concept)
A route that begins within an ovary or ovaries.	Preferred (foundation metadata concept)
A route that begins within or around the tissues surrounding the urethra.	Preferred (foundation metadata concept)
A route that begins within the abdomen.	Preferred (foundation metadata concept)
A route that begins within the bile duct and pancreatic duct.	Preferred (foundation metadata concept)
A route that begins within the bile, bile ducts or gallbladder.	Preferred (foundation metadata concept)
A route that begins within the bone.	Preferred (foundation metadata concept)
A route that begins within the breast.	Preferred (foundation metadata concept)
A route that begins within the canal of the cervix uteri.	Preferred (foundation metadata concept)
A route that begins within the channel of a tubular structure or tubular organ.	Preferred (foundation metadata concept)
A route that begins within the dermis of the skin.	Preferred (foundation metadata concept)
A route that begins within the dilatable spaces of the corpus cavernosa of the penis.	Preferred (foundation metadata concept)
A route that begins within the duct of a gland.	Preferred (foundation metadata concept)
A route that begins within the epidermis of the skin.	Preferred (foundation metadata concept)
A route that begins within the heart.	Preferred (foundation metadata concept)
A route that begins within the interstices of a tissue.	Preferred (foundation metadata concept)
A route that begins within the liver.	Preferred (foundation metadata concept)
A route that begins within the lymphatic vessels or nodes.	Preferred (foundation metadata concept)
A route that begins within the meninges.	Preferred (foundation metadata concept)
A route that begins within the myometrium.	Preferred (foundation metadata concept)
A route that begins within the periosteum.	Preferred (foundation metadata concept)
A route that begins within the pleura or pleural space.	Preferred (foundation metadata concept)
A route that begins within the prostate gland.	Preferred (foundation metadata concept)
A route that begins within the respiratory tract, including the oropharynx and nasopharynx.	Preferred (foundation metadata concept)
A route that begins within the skull.	Preferred (foundation metadata concept)
A route that begins within the testicles (male reproductive glands).	Preferred (foundation metadata concept)
A route that begins within the thorax internal to the ribs.	Preferred (foundation metadata concept)
A route that begins within the tissues surrounding a joint.	Preferred (foundation metadata concept)
A route that begins within the urethra.	Preferred (foundation metadata concept)
A route that begins within the vertebral column.	Preferred (foundation metadata concept)
A route that occurs outside of the body.	Preferred (foundation metadata concept)
A route used for extracorporeal haemodialysis where the product interacts with the patient blood through a semipermeable membrane.	Preferred (foundation metadata concept)
A route where the substance is placed directly into the lumen of a catheter, often to remedy or prevent an occlusion within the lumen of the catheter. The substance is not meant to directly interact with the patient and may be removed after a specified period of time.	Preferred (foundation metadata concept)
A safeguarding concern is a worry, anxiety or suspicion that a child or adult may be at risk of abuse or neglect, or that the individual may already have been harmed by a caregiver, institution or someone else they have contact with.	Preferred (foundation metadata concept)
A scan ultrasound	Acceptable (foundation metadata concept)
A scheduled procedure that is not performed on the scheduled procedure day and the decision not to perform the procedure takes place after anaesthesia induction time but before procedure/surgery start time.	Preferred (foundation metadata concept)
A scheduled procedure that is not performed on the scheduled procedure day and the decision not to perform the procedure takes place after anaesthesia start time but before anaesthesia induction time.	Preferred (foundation metadata concept)
A scheduled procedure that is not performed on the scheduled procedure day and the decision not to perform the procedure takes place before anaesthesia start time.	Preferred (foundation metadata concept)
A sclerosing disorder of the skeleton with increased bone density that classically displays the radiographic sign of sandwich vertebrae (dense bands of sclerosis parallel to the vertebral endplates). Onset of the disease is typically in late childhood or adolescence. The main manifestations are confined to the skeleton, including fractures, scoliosis, hip osteoarthritis and osteomyelitis, particularly affecting the mandible in association with dental abscess or caries. The disease is caused by heterozygous mutations in the chloride channel 7 (ClCN7) gene (16p13).	Preferred (foundation metadata concept)
A score for hospitalised patients which predicts the risk of patients returning for avoidable reasons.	Preferred (foundation metadata concept)
A scraping away of thin sections	Preferred (foundation metadata concept)
A screening test that determines the side of iliosacral somatic dysfunction (motion of ilium on the sacrum).	Preferred (foundation metadata concept)
A screening test that determines the side of sacroiliac somatic dysfunction (motion of the sacrum on the ilium).	Preferred (foundation metadata concept)
A semi-dominant X-linked disease with intellectual deficiency and seizures that is more severe in male patients. Boys presenting with lissencephaly show an abnormally thick cortex with very few gyri (pachygyria) or even none (agyria). Clinical manifestations include swallowing and feeding difficulties, abnormal muscular tone, seizures and severe to profound psychomotor retardation. Female patients display a less severe malformation referred to as doublecortex or subcortical laminar heterotopia and present with clinical signs of variable severity ranging from mild epilepsy to refractory epileptic seizures and severe intellectual deficiency. The condition is caused by doublecortin (DCX, located at Xq22.3-q23) gene mutations.	Preferred (foundation metadata concept)
A semi-solid dose form consisting of a hydrophilic gel.	Preferred (foundation metadata concept)
A semi-solid dose form consisting of a single-phase in which solids or liquids may be dissolved or dispersed in the base, which may be hydrophilic, hydrophobic or water-emulsifying.	Preferred (foundation metadata concept)
A semi-solid dose form consisting of solid particles finely dispersed in a suitable base.	Preferred (foundation metadata concept)
A semi-solid dose form of homogeneous appearance consisting of a lipophilic phase and an aqueous phase, one of which is finely dispersed in the other. Active substance(s) are dissolved or dispersed in the basis, which may be hydrophilic or hydrophobic.	Preferred (foundation metadata concept)
A semi-solid preparation consisting of a hydrophilic heat-retentive basis in which solid or liquid active substance(s) are dispersed.	Preferred (foundation metadata concept)
A separation of different structures along natural cleavage lines by dividing the connective tissue framework.	Preferred (foundation metadata concept)
A series of three dimensional ultrasound images continuously refreshed in real time resulting in a live motion video stream.	Preferred (foundation metadata concept)
A series of three dimensional ultrasound images of the heart continuously refreshed in real time resulting in a live motion video stream.	Preferred (foundation metadata concept)
A series prostaglandin	Preferred (foundation metadata concept)
A series prostaglandin (substance)	Preferred (foundation metadata concept)
A series prostaglandin adverse reaction	Preferred (foundation metadata concept)
A series prostaglandin adverse reaction (disorder)	Preferred (foundation metadata concept)
A series prostaglandin allergy	Acceptable (foundation metadata concept)
A series prostaglandin-containing product	Preferred (foundation metadata concept)
A serotype	Preferred (foundation metadata concept)
A serotype (qualifier value)	Preferred (foundation metadata concept)
A serotypes	Acceptable (foundation metadata concept)
A service of medicine focused on restoring health and functional abilities after acute illness or injury.	Preferred (foundation metadata concept)
A severe X-linked recessive neurodevelopmental disorder with the association of arthrogryposis multiplex congenita and intellectual disability. The syndrome has been reported in 5 families to date, with fewer than 30 affected individuals described. Affected patients are male, while carrier females are often asymptomatic. Facial weakness (ptosis) and bulbar weakness (feeding difficulty), characteristic dysmorphic facial and skeletal abnormalities have been reported. Other neurological signs may include spasticity and seizures. Heterozygous female carriers may also be affected, but to a lesser degree (intellectual disability, distal muscle weakness, camptodactyly, joint contractures, and pes equinovarus). Caused by mutations in the ZC4H2 gene (Xq11.1) that is presumed to play a role in neuronal function during fetal growth.	Preferred (foundation metadata concept)
A severe and rare form of systemic mastocytosis with manifestation of considerable infiltration of mast cells in different tissues. It represents less than 10% of cases of systemic mastocytosis. This disease doesn't usually develop in children. Cutaneous involvement is normally absent. Patients present with severe symptoms related to mast cell invasion and the intense release of mediators including syncope, recurrent flushing, organomegaly and organ dysfunction. The most serious complication is potentially fatal anaphylactic shock.There is evidence of an activating mutation of KIT, usually D816V, in the mast cells of the vast majority of patients. The prognosis is poor with a median survival of 2 to 4 years.	Preferred (foundation metadata concept)
A severe anomaly of bile acid synthesis with manifestation of severe neonatal cholestatic liver disease. To date, only 2 cases of this disorder have been reported. Caused by mutations in the 7-alpha hydroxylase gene (CYP7B1, 8q21.3). The deficiency in oxysterol 7-alpha-hydroxylation leads to the accumulation of hepatotoxic unsaturated monohydroxy bile acids. The mode of transmission is presumed to be autosomal recessive.	Preferred (foundation metadata concept)
A severe condition with onset in infancy of encephalomyopathy and in many cases renal tubulopathy. Manifestations include hypotonia, failure to thrive, microcephaly, and difficulty controlling head movement, delayed motor skills, serious breathing difficulties and can result in life-threatening respiratory failure. Most affected infants have lactic acidosis, which may also be life-threatening. Also associated are gastrointestinal dysmotility, seizures and sensorineural hearing loss. The disease is caused by mutations in the RRM2B gene which provides instructions for making one piece of the protein ribonucleotide reductase (RNR). RRM2B gene mutations reduce the activity or amount of RNR, which likely impairs production of mitochondrial DNA nucleotides. Inherited in an autosomal recessive pattern.	Preferred (foundation metadata concept)
A severe congenital systemic autoimmune disease characterised by refractory diarrhoea, endocrinopathies, cutaneous involvement and infections. The syndrome usually develops during the first few days or weeks of life and affects exclusively boys. Caused by mutations in the FOXP3 gene (Xp11.23). This gene codes for a forkhead transcription factor which controls the development and function of CD4+ CD25+ regulatory T cells, a major lymphocyte population involved in downregulation of immune responses and self-tolerance. Transmission is X-linked recessive.	Preferred (foundation metadata concept)

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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)