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

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:

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)

1233160 members. Search Members:

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
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 Acceptable (foundation metadata concept)
9am cortisol level Preferred (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)
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)
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)
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)

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