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
29 (AJCC)	Acceptable (foundation metadata concept)
29 (UICC)	Acceptable (foundation metadata concept)
29 (qualifier value)	Preferred (foundation metadata concept)
290	Preferred (foundation metadata concept)
290 (qualifier value)	Preferred (foundation metadata concept)
291.667	Preferred (foundation metadata concept)
291.667 (qualifier value)	Preferred (foundation metadata concept)
29E	Preferred (foundation metadata concept)
29G	Preferred (foundation metadata concept)
29G (qualifier value)	Preferred (foundation metadata concept)
2A (AJCC)	Acceptable (foundation metadata concept)
2A (UICC)	Acceptable (foundation metadata concept)
2A1 (AJCC)	Acceptable (foundation metadata concept)
2A1 (UICC)	Acceptable (foundation metadata concept)
2A2 (AJCC)	Acceptable (foundation metadata concept)
2A2 (UICC)	Acceptable (foundation metadata concept)
2B (AJCC)	Acceptable (foundation metadata concept)
2B (UICC)	Acceptable (foundation metadata concept)
2C (AJCC)	Acceptable (foundation metadata concept)
2C (UICC)	Acceptable (foundation metadata concept)
2D (two dimensional) external beam radiation therapy involves dose calculation without projection onto 3D imaging and delivered without 3D techniques.	Preferred (foundation metadata concept)
2D (two dimensional) external beam radiotherapy	Acceptable (foundation metadata concept)
2D (two dimensional) mode ultrasound - action	Preferred (foundation metadata concept)
2D-EBRT - two dimensional external beam radiation therapy	Acceptable (foundation metadata concept)
2E (AJCC)	Acceptable (foundation metadata concept)
2E (UICC)	Acceptable (foundation metadata concept)
2H post 100 g glucose PO	Acceptable (foundation metadata concept)
2H post 75 g glucose PO	Acceptable (foundation metadata concept)
2H post dose glucose	Acceptable (foundation metadata concept)
2H post incubation	Acceptable (foundation metadata concept)
2H post meal	Acceptable (foundation metadata concept)
2H post peritoneal dialysis	Acceptable (foundation metadata concept)
2H specimen	Acceptable (foundation metadata concept)
2H4	Acceptable (foundation metadata concept)
2a	Preferred (foundation metadata concept)
2a (qualifier value)	Preferred (foundation metadata concept)
2b	Preferred (foundation metadata concept)
2b (qualifier value)	Preferred (foundation metadata concept)
2g protein exchanges/day	Preferred (foundation metadata concept)
2g protein exchanges/day (qualifier value)	Preferred (foundation metadata concept)
2g protein exchanges/kg body weight	Preferred (foundation metadata concept)
2g protein exchanges/kg body weight (qualifier value)	Preferred (foundation metadata concept)
2g protein exchanges/meal	Preferred (foundation metadata concept)
2g protein exchanges/meal (qualifier value)	Preferred (foundation metadata concept)
2nd	Acceptable (foundation metadata concept)
2nd HiB and DTP vaccine given	Preferred (foundation metadata concept)
2nd HiB and DTP vaccine given (situation)	Preferred (foundation metadata concept)
2nd Hib and DTP vaccine given	Preferred (foundation metadata concept)
2nd Japanese encephalitis vaccination	Preferred (foundation metadata concept)
2nd Japanese encephalitis vaccination	Preferred (foundation metadata concept)
2nd Japanese encephalitis vaccination (procedure)	Preferred (foundation metadata concept)
2nd Japanese encephalitis vaccination (procedure)	Preferred (foundation metadata concept)
2nd floor	Acceptable (foundation metadata concept)
2nd heart sound split	Acceptable (foundation metadata concept)
2nd hepatitis A junior vaccination	Acceptable (foundation metadata concept)
2nd left lumbar vein	Acceptable (foundation metadata concept)
2nd right lumbar vein	Acceptable (foundation metadata concept)
2nd specimen	Acceptable (foundation metadata concept)
2nd stage of labour length	Acceptable (foundation metadata concept)
2nd stage of labour length	Preferred (foundation metadata concept)
2nd stage of labour length (observable entity)	Preferred (foundation metadata concept)
2nd trimester	Acceptable (foundation metadata concept)
2p partial trisomy syndrome	Preferred (foundation metadata concept)
2p partial trisomy syndrome (disorder)	Preferred (foundation metadata concept)
2p13.2 microdeletion syndrome	Preferred (foundation metadata concept)
2p13.2 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
2p15p16.1 microdeletion syndrome	Preferred (foundation metadata concept)
2p15p16.1 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
2p15p16.1 microdeletion syndrome is a recently described syndrome characterised by developmental delay and facial dysmorphism.	Preferred (foundation metadata concept)
2p21 microdeletion syndrome	Preferred (foundation metadata concept)
2p21 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
2p21 microdeletion syndrome without cystinuria	Preferred (foundation metadata concept)
2p21 microdeletion syndrome without cystinuria (disorder)	Preferred (foundation metadata concept)
2p21 microdeletion syndrome without cystinuria is a rare partial autosomal monosomy characterised by weak fetal movements, severe infantile hypotonia and feeding difficulties that spontaneously improve with time, urogenital abnormalities (hypospadias or hypoplastic labia majora), global development delay, mild intellectual disability and facial dysmorphism (dolichocephaly, frontal bossing, bilateral ptosis, midface retrusion, open mouth with tented upper lip vermilion). Affected individuals have borderline elevated serum lactate but no cystinuria.	Preferred (foundation metadata concept)
2q partial trisomy syndrome	Preferred (foundation metadata concept)
2q partial trisomy syndrome (disorder)	Preferred (foundation metadata concept)
2q23.1 microdeletion syndrome	Preferred (foundation metadata concept)
2q23.1 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
2q23.1 microduplication syndrome	Preferred (foundation metadata concept)
2q23.1 microduplication syndrome (disorder)	Preferred (foundation metadata concept)
2q23.1 microduplication syndrome is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the long arm of chromosome 2, primarily characterised by global developmental delay, hypotonia, autistic-like features and behavioural problems. Craniofacial dysmorphism (arched eyebrows, hypertelorism, bilateral ptosis, prominent nose, wide mouth, micro/retrognathia) and an affable personality are also commonly associated. Minor digital anomalies (fifth finger clinodactyly and large, broad first toe) have occasionally been reported.	Preferred (foundation metadata concept)
2q24 microdeletion syndrome	Preferred (foundation metadata concept)
2q24 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
2q24 microdeletion syndrome is a chromosomal anomaly consisting of a partial long arm deletion of chromosome 2 and characterised clinically by a wide range of manifestations (depending on the specific region deleted) which can include seizures, microcephaly, dysmorphic features, cleft palate, eye abnormalities (coloboma, cataract and microphthalmia), growth retardation, failure to thrive, heart defects, limb anomalies, developmental delay and autism.	Preferred (foundation metadata concept)
2q31.1 microdeletion syndrome	Preferred (foundation metadata concept)
2q31.1 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
2q31.1 microdeletion syndrome is a well-defined and clinically recognisable syndrome characterised by moderate to severe developmental delay, short stature, facial dysmorphism and variable limb defects.	Preferred (foundation metadata concept)
2q32q33 microdeletion syndrome	Preferred (foundation metadata concept)
2q32q33 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
2q33.1 microdeletion syndrome	Preferred (foundation metadata concept)
2q33.1 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
2q37 deletion syndrome	Acceptable (foundation metadata concept)
2x normal saline 1.8% infusion solution bag	Acceptable (foundation metadata concept)
2x/wk	Acceptable (foundation metadata concept)
3	Preferred (foundation metadata concept)
3	Preferred (foundation metadata concept)
3 (AJCC)	Acceptable (foundation metadata concept)
3 (UICC)	Acceptable (foundation metadata concept)
3 (qualifier value)	Preferred (foundation metadata concept)
3 Buck shot	Preferred (foundation metadata concept)
3 Buck shot, device	Acceptable (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)