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
78-As	Acceptable (foundation metadata concept)
78-Ge	Acceptable (foundation metadata concept)
78V-2441 virus	Preferred (foundation metadata concept)
78V-2441 virus (organism)	Preferred (foundation metadata concept)
78V-3531 virus	Preferred (foundation metadata concept)
78V-3531 virus (organism)	Preferred (foundation metadata concept)
79-Kr	Acceptable (foundation metadata concept)
79-Se	Acceptable (foundation metadata concept)
7D post incubation	Acceptable (foundation metadata concept)
7Fr	Acceptable (foundation metadata concept)
7alpha-hydroxysteroid dehydrogenase	Preferred (foundation metadata concept)
7alpha-hydroxysteroid dehydrogenase (substance)	Preferred (foundation metadata concept)
7beta-hydroxysteroid dehydrogenase (NADP^+^)	Acceptable (foundation metadata concept)
7beta-hydroxysteroid dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^)	Preferred (foundation metadata concept)
7beta-hydroxysteroid dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^) (substance)	Preferred (foundation metadata concept)
7g protein exchanges/day	Preferred (foundation metadata concept)
7g protein exchanges/day (qualifier value)	Preferred (foundation metadata concept)
7g protein exchanges/kg body weight	Preferred (foundation metadata concept)
7g protein exchanges/kg body weight (qualifier value)	Preferred (foundation metadata concept)
7g protein exchanges/meal	Preferred (foundation metadata concept)
7g protein exchanges/meal (qualifier value)	Preferred (foundation metadata concept)
7p partial monosomy	Preferred (foundation metadata concept)
7p partial monosomy (disorder)	Preferred (foundation metadata concept)
7p partial trisomy	Preferred (foundation metadata concept)
7p partial trisomy (disorder)	Preferred (foundation metadata concept)
7p12-p14 deletion syndrome	Preferred (foundation metadata concept)
7p12-p14 deletion syndrome (disorder)	Preferred (foundation metadata concept)
7p21.1 deletion syndrome	Preferred (foundation metadata concept)
7p21.1 deletion syndrome (disorder)	Preferred (foundation metadata concept)
7p22.1 microduplication syndrome	Preferred (foundation metadata concept)
7p22.1 microduplication syndrome (disorder)	Preferred (foundation metadata concept)
7p22.1 microduplication syndrome is a rare chromosomal anomaly syndrome, resulting from a partial interstitial microduplication of the short arm of chromosome 7, characterised by intellectual disability, psychomotor and speech delays, craniofacial dysmorphism (including macrocephaly, frontal bossing, hypertelorism, abnormally slanted palpebral fissures, anteverted nares, low-set ears, microretrognathia) and cryptorchidism. Cardiac (e.g., patent foramen ovale and atrial septal defect), as well as renal, skeletal and ocular abnormalities may also be associated.	Preferred (foundation metadata concept)
7q partial monosomy	Preferred (foundation metadata concept)
7q partial monosomy (disorder)	Preferred (foundation metadata concept)
7q partial trisomy	Preferred (foundation metadata concept)
7q partial trisomy (disorder)	Preferred (foundation metadata concept)
7q11.23 microduplication syndrome	Preferred (foundation metadata concept)
7q11.23 microduplication syndrome (disorder)	Preferred (foundation metadata concept)
7q11.23 microduplication syndrome is a rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 7 characterised by a highly variable phenotype that typically manifests with mild-moderate intellectual delay (patients could be in the normal range), speech disorders (particularly of expressive language), and distinctive craniofacial features (brachycephaly, broad forehead, straight eyebrows, broad nasal tip, short philtrum, thin upper lip and facial asymmetry). Hypotonia, developmental coordination disorders, behavioural problems (such as anxiety, ADHD and oppositional disorders) and various congenital anomalies, such as heart defects, diaphragmatic hernia, renal malformations and cryptorchidism, are frequently presented. Neurological abnormalities (visible on MRI) have been reported.	Preferred (foundation metadata concept)
7q31 microdeletion syndrome	Preferred (foundation metadata concept)
7q31 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
7q31 microdeletion syndrome is a rare chromosomal anomaly characterised by speech and language disorder, predominantly presenting as an apraxia of speech, sometimes associated with oral motor dyspraxia, dysarthria, receptive and expressive language disorder, and hearing loss. Individuals with larger deletions in this region have also been reported to display intellectual disability and autism.	Preferred (foundation metadata concept)
7q36.3 microduplication syndrome	Acceptable (foundation metadata concept)
7s IgM	Acceptable (foundation metadata concept)
7th floor	Acceptable (foundation metadata concept)
8	Preferred (foundation metadata concept)
8	Preferred (foundation metadata concept)
8 (qualifier value)	Preferred (foundation metadata concept)
8 French gauge	Preferred (foundation metadata concept)
8 French gauge (qualifier value)	Preferred (foundation metadata concept)
8 hour urine specimen	Preferred (foundation metadata concept)
8 hours	Preferred (foundation metadata concept)
8 hours (qualifier value)	Preferred (foundation metadata concept)
8 mm caliber bullet, device	Acceptable (foundation metadata concept)
8 mm caliber bullet, device (physical object)	Preferred (foundation metadata concept)
8 mm calibre bullet	Preferred (foundation metadata concept)
8 month examination abnormal - for observation	Preferred (foundation metadata concept)
8 month examination abnormal - for observation (finding)	Preferred (foundation metadata concept)
8 month examination abnormal - on treatment	Preferred (foundation metadata concept)
8 month examination abnormal - on treatment (finding)	Preferred (foundation metadata concept)
8 month examination abnormal - referred	Preferred (foundation metadata concept)
8 month examination abnormal - referred (finding)	Preferred (foundation metadata concept)
8 o'clock position	Preferred (foundation metadata concept)
8 o'clock position (qualifier value)	Preferred (foundation metadata concept)
8 o'clock position on mammogram	Preferred (foundation metadata concept)
8 o'clock position on mammogram (finding)	Preferred (foundation metadata concept)
8 week examination abnormal - for observation	Preferred (foundation metadata concept)
8 week examination abnormal - for observation	Preferred (foundation metadata concept)
8 week examination abnormal - for observation (finding)	Preferred (foundation metadata concept)
8 week examination abnormal - for observation (finding)	Preferred (foundation metadata concept)
8 week examination abnormal - on treatment	Preferred (foundation metadata concept)
8 week examination abnormal - on treatment	Preferred (foundation metadata concept)
8 week examination abnormal - on treatment (finding)	Preferred (foundation metadata concept)
8 week examination abnormal - on treatment (finding)	Preferred (foundation metadata concept)
8 week examination abnormal - referred	Preferred (foundation metadata concept)
8 week examination abnormal - referred	Preferred (foundation metadata concept)
8 week examination abnormal - referred (finding)	Preferred (foundation metadata concept)
8 week examination abnormal - referred (finding)	Preferred (foundation metadata concept)
8,11,14-eicosatrienoic acid	Preferred (foundation metadata concept)
8,11,14-eicosatrienoic acid (substance)	Preferred (foundation metadata concept)
8-9 month exam normal	Preferred (foundation metadata concept)
8-9 month exam normal	Preferred (foundation metadata concept)
8-9 month exam normal (finding)	Preferred (foundation metadata concept)
8-9 month exam normal (finding)	Preferred (foundation metadata concept)
8-9 month exam not attended	Preferred (foundation metadata concept)
8-9 month exam not attended	Preferred (foundation metadata concept)
8-9 month exam not attended (situation)	Preferred (foundation metadata concept)
8-9 month exam not attended (situation)	Preferred (foundation metadata concept)
8-9 month exam not offered	Preferred (foundation metadata concept)
8-9 month exam not offered	Preferred (foundation metadata concept)
8-9 month exam not offered (situation)	Preferred (foundation metadata concept)
8-9 month exam not offered (situation)	Preferred (foundation metadata concept)
8-9 month exam not wanted	Preferred (foundation metadata concept)
8-9 month exam not wanted	Preferred (foundation metadata concept)
8-9 month exam not wanted (situation)	Preferred (foundation metadata concept)
8-9 month exam not wanted (situation)	Preferred (foundation metadata concept)
8-9 month examination abnormal - for observation	Preferred (foundation metadata concept)
8-9 month examination abnormal - for observation (finding)	Preferred (foundation metadata concept)
8-9 month examination abnormal - on treatment	Preferred (foundation metadata concept)
8-9 month examination abnormal - on treatment (finding)	Preferred (foundation metadata concept)
8-9 month examination abnormal - referred	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)