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
14-C Aminopyrine solution	Acceptable (foundation metadata concept)
14-C Glycocholic acid solution	Acceptable (foundation metadata concept)
14-C Triolein solution	Acceptable (foundation metadata concept)
14-DAY FLEA AND TICK SPRAY	Preferred (foundation metadata concept)
14-DAY FLEA AND TICK SPRAY (product)	Preferred (foundation metadata concept)
14-O	Acceptable (foundation metadata concept)
14-hydroxyclarithromycin	Preferred (foundation metadata concept)
14-hydroxyclarithromycin (substance)	Preferred (foundation metadata concept)
14-hydroxydihydrocodeinone	Acceptable (foundation metadata concept)
140	Preferred (foundation metadata concept)
140 (qualifier value)	Preferred (foundation metadata concept)
14000	Preferred (foundation metadata concept)
14000 (qualifier value)	Preferred (foundation metadata concept)
1409/69	Preferred (foundation metadata concept)
141	Preferred (foundation metadata concept)
141 (qualifier value)	Preferred (foundation metadata concept)
1413 U	Preferred (foundation metadata concept)
143	Preferred (foundation metadata concept)
143 (qualifier value)	Preferred (foundation metadata concept)
143.75	Preferred (foundation metadata concept)
143.75 (qualifier value)	Preferred (foundation metadata concept)
1432	Preferred (foundation metadata concept)
1432 (qualifier value)	Preferred (foundation metadata concept)
144	Preferred (foundation metadata concept)
144 (qualifier value)	Preferred (foundation metadata concept)
144.6	Preferred (foundation metadata concept)
144.6 (qualifier value)	Preferred (foundation metadata concept)
1440	Preferred (foundation metadata concept)
1440 (qualifier value)	Preferred (foundation metadata concept)
145	Preferred (foundation metadata concept)
145 (qualifier value)	Preferred (foundation metadata concept)
146-Gd	Acceptable (foundation metadata concept)
147-Gd	Acceptable (foundation metadata concept)
1473 K	Preferred (foundation metadata concept)
148-Gd	Acceptable (foundation metadata concept)
149	Preferred (foundation metadata concept)
149 (qualifier value)	Preferred (foundation metadata concept)
149-Gd	Acceptable (foundation metadata concept)
14C urea breath test	Preferred (foundation metadata concept)
14C urea breath test (procedure)	Preferred (foundation metadata concept)
14G	Preferred (foundation metadata concept)
14G (qualifier value)	Preferred (foundation metadata concept)
14q partial distal trisomy syndrome	Preferred (foundation metadata concept)
14q partial distal trisomy syndrome (disorder)	Preferred (foundation metadata concept)
14q partial proximal trisomy syndrome	Preferred (foundation metadata concept)
14q partial proximal trisomy syndrome (disorder)	Preferred (foundation metadata concept)
14q partial trisomy	Preferred (foundation metadata concept)
14q partial trisomy (disorder)	Preferred (foundation metadata concept)
14q11.2 microdeletion syndrome	Preferred (foundation metadata concept)
14q11.2 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
14q11.2 microdeletion syndrome is a recently described syndrome characterised by developmental delay, hypotonia and facial dysmorphism.	Preferred (foundation metadata concept)
14q11.2 microduplication syndrome	Preferred (foundation metadata concept)
14q11.2 microduplication syndrome (disorder)	Preferred (foundation metadata concept)
14q11.2 microduplication syndrome is a rare chromosomal anomaly characterised by developmental delay, mild to severe intellectual disability with speech impairment and epilepsy. Additionally, it may include dysmorphic features (such as hypo- or hypertelorism, dysplastic ears, short palpebral fissures), microcephaly or macrocephaly, behavioural abnormalities, stereotyped hand movements, ataxia, hypotonia, cleft palate.	Preferred (foundation metadata concept)
14q12 microdeletion syndrome	Preferred (foundation metadata concept)
14q12 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
14q12 microdeletion syndrome is a recently described syndrome characterised by severe intellectual deficit, with a normal neonatal period, followed by a phase of regression at the age of 3-6 months.	Preferred (foundation metadata concept)
14q22-q23 microdeletion syndrome	Acceptable (foundation metadata concept)
14q22q23 microdeletion syndrome	Preferred (foundation metadata concept)
14q22q23 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
14q22q23 microdeletion syndrome is a rare partial deletion of the long arm of chromosome 14 characterised by ocular anomalies (anophthalmia/microphthalmia, ptosis, hypertelorism, exophthalmos), pituitary anomalies (pituitary hypoplasia/aplasia with growth hormone deficiency and growth retardation) and hand/foot anomalies (polydactyly, short digits, pes cavus). Other clinical features may include muscular hypotonia, psychomotor development delay/intellectual disability, dysmorphic signs (facial asymmetry, microretrognathia, high-arched palate, ear anomalies), congenital genitourinary malformations, hearing impairment. Smaller 14q22 deletions may have variable expression.	Preferred (foundation metadata concept)
14q24.1q24.3 microdeletion syndrome	Preferred (foundation metadata concept)
14q24.1q24.3 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
14q24.1q24.3 microdeletion syndrome is a rare, genetic, syndromic intellectual disability characterised by mild intellectual disability, delayed speech development, congenital heart defects, brachydactyly and dysmorphic facial features.	Preferred (foundation metadata concept)
14q32 deletion syndrome	Preferred (foundation metadata concept)
14q32 deletion syndrome (disorder)	Preferred (foundation metadata concept)
14q32 duplication syndrome	Preferred (foundation metadata concept)
14q32 duplication syndrome (disorder)	Preferred (foundation metadata concept)
14q32 duplication syndrome is a rare chromosomal anomaly syndrome resulting from the partial duplication of the long arm of chromosome 14 that results in a predisposition to a number of adult-onset myeloproliferative neoplasms, including acute myeloid leukaemia, chronic myelomonocytic leukaemia, and especially essential thrombocythaemia. Progression to myelofibrosis and secondary acute myeloid leukaemia can be observed.	Preferred (foundation metadata concept)
15	Preferred (foundation metadata concept)
15 (AJCC)	Acceptable (foundation metadata concept)
15 (UICC)	Acceptable (foundation metadata concept)
15 (qualifier value)	Preferred (foundation metadata concept)
15 French gauge	Preferred (foundation metadata concept)
15 French gauge (qualifier value)	Preferred (foundation metadata concept)
15 lead electrocardiographic monitoring	Preferred (foundation metadata concept)
15 lead electrocardiographic monitoring (procedure)	Preferred (foundation metadata concept)
15 minutes post-dose	Preferred (foundation metadata concept)
15 minutes post-dose (qualifier value)	Preferred (foundation metadata concept)
15 year examination	Preferred (foundation metadata concept)
15 year examination	Preferred (foundation metadata concept)
15 year examination	Preferred (foundation metadata concept)
15 year examination (procedure)	Preferred (foundation metadata concept)
15 year examination (procedure)	Preferred (foundation metadata concept)
15 year examination (procedure)	Preferred (foundation metadata concept)
15 year examination NOS	Preferred (foundation metadata concept)
15 year examination NOS	Preferred (foundation metadata concept)
15 year examination NOS (procedure)	Preferred (foundation metadata concept)
15 year examination NOS (situation)	Preferred (foundation metadata concept)
15 year examination abnormal - for observation	Preferred (foundation metadata concept)
15 year examination abnormal - for observation	Preferred (foundation metadata concept)
15 year examination abnormal - for observation (finding)	Preferred (foundation metadata concept)
15 year examination abnormal - for observation (finding)	Preferred (foundation metadata concept)
15 year examination abnormal - on treatment	Preferred (foundation metadata concept)
15 year examination abnormal - on treatment	Preferred (foundation metadata concept)
15 year examination abnormal - on treatment (finding)	Preferred (foundation metadata concept)
15 year examination abnormal - on treatment (finding)	Preferred (foundation metadata concept)
15 year examination abnormal - referred	Preferred (foundation metadata concept)
15 year examination abnormal - referred	Preferred (foundation metadata concept)
15 year examination abnormal - referred (finding)	Preferred (foundation metadata concept)
15 year examination abnormal - referred (finding)	Preferred (foundation metadata concept)

Start Previous Page 70 of 13273 Next End

Reference Sets

Reference set descriptor

Back to Start

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)