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
960	Preferred (foundation metadata concept)
960 (qualifier value)	Preferred (foundation metadata concept)
96000000	Preferred (foundation metadata concept)
96000000 (qualifier value)	Preferred (foundation metadata concept)
97	Preferred (foundation metadata concept)
97 (qualifier value)	Preferred (foundation metadata concept)
97-Ru	Acceptable (foundation metadata concept)
97-Tc	Acceptable (foundation metadata concept)
97-Zr	Acceptable (foundation metadata concept)
97.2	Preferred (foundation metadata concept)
97.2 (qualifier value)	Preferred (foundation metadata concept)
975	Preferred (foundation metadata concept)
975 (qualifier value)	Preferred (foundation metadata concept)
97m-Tc	Acceptable (foundation metadata concept)
98	Preferred (foundation metadata concept)
98 (qualifier value)	Preferred (foundation metadata concept)
98-Tc	Acceptable (foundation metadata concept)
980	Preferred (foundation metadata concept)
980 (qualifier value)	Preferred (foundation metadata concept)
99	Preferred (foundation metadata concept)
99 (qualifier value)	Preferred (foundation metadata concept)
99-Mo	Acceptable (foundation metadata concept)
99-Rh	Acceptable (foundation metadata concept)
99-Tc	Acceptable (foundation metadata concept)
99.5	Preferred (foundation metadata concept)
99.5 (qualifier value)	Preferred (foundation metadata concept)
99.74	Preferred (foundation metadata concept)
99.74 (qualifier value)	Preferred (foundation metadata concept)
99.9	Preferred (foundation metadata concept)
99.9 (qualifier value)	Preferred (foundation metadata concept)
99.96	Preferred (foundation metadata concept)
99.96 (qualifier value)	Preferred (foundation metadata concept)
990	Preferred (foundation metadata concept)
990 (qualifier value)	Preferred (foundation metadata concept)
999	Preferred (foundation metadata concept)
999 (qualifier value)	Preferred (foundation metadata concept)
999.34	Preferred (foundation metadata concept)
999.34 (qualifier value)	Preferred (foundation metadata concept)
99m-Rh	Acceptable (foundation metadata concept)
99m-Tc	Acceptable (foundation metadata concept)
99mTc-HMPAO	Acceptable (foundation metadata concept)
9Fr	Acceptable (foundation metadata concept)
9am cortisol level	Preferred (foundation metadata concept)
9am cortisol level	Acceptable (foundation metadata concept)
9am cortisol level	Preferred (foundation metadata concept)
9am cortisol level (procedure)	Preferred (foundation metadata concept)
9am cortisol level (procedure)	Preferred (foundation metadata concept)
9am cortisol measurement	Preferred (foundation metadata concept)
9am cortisol measurement (procedure)	Preferred (foundation metadata concept)
9p deletion syndrome	Acceptable (foundation metadata concept)
9p minus syndrome	Acceptable (foundation metadata concept)
9p monosomy syndrome	Acceptable (foundation metadata concept)
9p partial monosomy syndrome	Preferred (foundation metadata concept)
9p partial monosomy syndrome (disorder)	Preferred (foundation metadata concept)
9p partial trisomy syndrome	Preferred (foundation metadata concept)
9p partial trisomy syndrome (disorder)	Preferred (foundation metadata concept)
9p13 microdeletion syndrome	Preferred (foundation metadata concept)
9p13 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
9p13 microdeletion syndrome is a rare chromosomal anomaly syndrome, resulting from a partial interstitial deletion of the short arm of chromosome 9, characterised by mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivity disorder and a social personality. Patients also present bruxism, short stature and minor facial dysmorphic features (e.g., bilateral epicanthic folds, broad, flat nasal bridge, anteverted nares, low-set ears micro/retro-gnathia).	Preferred (foundation metadata concept)
9p24.3 deletion syndrome	Preferred (foundation metadata concept)
9p24.3 deletion syndrome (disorder)	Preferred (foundation metadata concept)
9q partial monosomy syndrome	Preferred (foundation metadata concept)
9q partial monosomy syndrome (disorder)	Preferred (foundation metadata concept)
9q partial trisomy syndrome	Preferred (foundation metadata concept)
9q partial trisomy syndrome (disorder)	Preferred (foundation metadata concept)
9q21.13 microdeletion syndrome	Preferred (foundation metadata concept)
9q21.13 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
9q22.3 deletion syndrome	Acceptable (foundation metadata concept)
9q22.3 deletion syndrome	Preferred (foundation metadata concept)
9q22.3 deletion syndrome (disorder)	Preferred (foundation metadata concept)
9q31.1q31.3 microdeletion syndrome	Preferred (foundation metadata concept)
9q31.1q31.3 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
9q31.1q31.3 microdeletion syndrome is a rare, genetic, syndromic intellectual disability characterised by mild intellectual disability, short stature with high body mass index, short neck with cervical gibbus and dysmorphic facial features. A metabolic syndrome, including type 2 diabetes, hypercholesterolaemia and hypertension has also been reported.	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)

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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)