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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)


1327206 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
121 (AJCC) Acceptable (foundation metadata concept)
121 (UICC) Acceptable (foundation metadata concept)
121-I Acceptable (foundation metadata concept)
121-Sn Acceptable (foundation metadata concept)
121-Te Acceptable (foundation metadata concept)
121m-Sn Acceptable (foundation metadata concept)
121m-Te Acceptable (foundation metadata concept)
122 (AJCC) Acceptable (foundation metadata concept)
122 (UICC) Acceptable (foundation metadata concept)
122-I Acceptable (foundation metadata concept)
122-Sb Acceptable (foundation metadata concept)
122-Xe Acceptable (foundation metadata concept)
123 (AJCC) Acceptable (foundation metadata concept)
123 (UICC) Acceptable (foundation metadata concept)
123-I Acceptable (foundation metadata concept)
123-Sn Acceptable (foundation metadata concept)
123-Xe Acceptable (foundation metadata concept)
123m-Te Acceptable (foundation metadata concept)
124 Preferred (foundation metadata concept)
124 (AJCC) Acceptable (foundation metadata concept)
124 (UICC) Acceptable (foundation metadata concept)
124 (qualifier value) Preferred (foundation metadata concept)
124-I Acceptable (foundation metadata concept)
124-Sb Acceptable (foundation metadata concept)
125 Preferred (foundation metadata concept)
125 (AJCC) Acceptable (foundation metadata concept)
125 (UICC) Acceptable (foundation metadata concept)
125 (qualifier value) Preferred (foundation metadata concept)
125-I Acceptable (foundation metadata concept)
125-Sb Acceptable (foundation metadata concept)
125-Sn Acceptable (foundation metadata concept)
125-Xe Acceptable (foundation metadata concept)
1250 Preferred (foundation metadata concept)
1250 (qualifier value) Preferred (foundation metadata concept)
12500 Preferred (foundation metadata concept)
12500 (qualifier value) Preferred (foundation metadata concept)
125000 Preferred (foundation metadata concept)
125000 (qualifier value) Preferred (foundation metadata concept)
125m-Te Acceptable (foundation metadata concept)
126 Preferred (foundation metadata concept)
126 (qualifier value) Preferred (foundation metadata concept)
126-Ba Acceptable (foundation metadata concept)
126-Cs Acceptable (foundation metadata concept)
126-I Acceptable (foundation metadata concept)
126-Sb Acceptable (foundation metadata concept)
127-Cs Acceptable (foundation metadata concept)
127-Sb Acceptable (foundation metadata concept)
127-Sn Acceptable (foundation metadata concept)
127-Te Acceptable (foundation metadata concept)
127-Xe Acceptable (foundation metadata concept)
127m-Te Acceptable (foundation metadata concept)
127m-Xe Acceptable (foundation metadata concept)
128-Ba Acceptable (foundation metadata concept)
128-Cs Acceptable (foundation metadata concept)
128-Sb Acceptable (foundation metadata concept)
129-Ba Acceptable (foundation metadata concept)
129-Cs Acceptable (foundation metadata concept)
129-I Acceptable (foundation metadata concept)
129-Sb Acceptable (foundation metadata concept)
129-Te Acceptable (foundation metadata concept)
129.167 Preferred (foundation metadata concept)
129.167 (qualifier value) Preferred (foundation metadata concept)
1295 Preferred (foundation metadata concept)
1295 (qualifier value) Preferred (foundation metadata concept)
129m-Te Acceptable (foundation metadata concept)
129m-Xe Acceptable (foundation metadata concept)
12Fr Acceptable (foundation metadata concept)
12G Preferred (foundation metadata concept)
12G (qualifier value) Preferred (foundation metadata concept)
12H post peritoneal dialysis Acceptable (foundation metadata concept)
12alpha-hydroxysteroid dehydrogenase Preferred (foundation metadata concept)
12alpha-hydroxysteroid dehydrogenase (substance) Preferred (foundation metadata concept)
12p partial monosomy syndrome Preferred (foundation metadata concept)
12p partial monosomy syndrome (disorder) Preferred (foundation metadata concept)
12p partial trisomy syndrome Preferred (foundation metadata concept)
12p partial trisomy syndrome (disorder) Preferred (foundation metadata concept)
12p12.1 microdeletion syndrome Preferred (foundation metadata concept)
12p12.1 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
12p13.33 microdeletion syndrome Acceptable (foundation metadata concept)
12q partial trisomy syndrome Preferred (foundation metadata concept)
12q partial trisomy syndrome (disorder) Preferred (foundation metadata concept)
12q14 microdeletion syndrome Preferred (foundation metadata concept)
12q14 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
12q14 microdeletion syndrome is characterised by mild intellectual deficit, failure to thrive, short stature and osteopoikilosis. It has been described in four unrelated patients. The syndrome appears to be caused by a heterozygous deletion at chromosome region 12q14, which was detected in three of the four patients. The deleted region contains the LEMD3 gene: mutations in this gene have already been implicated in osteopoikilosis. Preferred (foundation metadata concept)
12q15 deletion syndrome Preferred (foundation metadata concept)
12q15 deletion syndrome (disorder) Preferred (foundation metadata concept)
12q15q21.1 microdeletion syndrome Preferred (foundation metadata concept)
12q15q21.1 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
12q15q21.1 microdeletion syndrome is a rare chromosomal anomaly syndrome resulting from a partial deletion of the long arm of chromosome 12, with a highly variable phenotype, typically characterised by developmental delay, learning disability, intra-uterine and postnatal growth retardation, and mild facial dysmorphism that changes with age. Nasal speech and hypothyroidism are also associated. Preferred (foundation metadata concept)
12q24.31-q24.32 deletion syndrome Preferred (foundation metadata concept)
12q24.31-q24.32 deletion syndrome (disorder) Preferred (foundation metadata concept)
12x/day Acceptable (foundation metadata concept)
13 Preferred (foundation metadata concept)
13 (AJCC) Acceptable (foundation metadata concept)
13 (UICC) Acceptable (foundation metadata concept)
13 (qualifier value) Preferred (foundation metadata concept)
13 carbon to 12 carbon breath carbon dioxide ratio Acceptable (foundation metadata concept)
13 carbon to 12 carbon breath carbon dioxide ratio (procedure) Preferred (foundation metadata concept)
13 carbon to 12 carbon breath co2 ratio Acceptable (foundation metadata concept)
13 cis-Dodecenoic acid Preferred (foundation metadata concept)
13 cis-Dodecenoic acid (substance) Preferred (foundation metadata concept)

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