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900000000000509007: United States of America 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
900000000001115012 United States of America 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)
900000000001116013 US English en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)
900000000001117016 United States of America 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)


1317531 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
US English Is a English [International Organization for Standardization 639-1 code en] language reference set (foundation metadata concept) true Inferred relationship Some

Members acceptabilityId
29 (qualifier value) Preferred (foundation metadata concept)
290 Preferred (foundation metadata concept)
290 (qualifier value) Preferred (foundation metadata concept)
291.667 Preferred (foundation metadata concept)
291.667 (qualifier value) Preferred (foundation metadata concept)
29E Preferred (foundation metadata concept)
29G Preferred (foundation metadata concept)
29G (qualifier value) Preferred (foundation metadata concept)
2A (AJCC) Acceptable (foundation metadata concept)
2A (UICC) Acceptable (foundation metadata concept)
2A1 (AJCC) Acceptable (foundation metadata concept)
2A1 (UICC) Acceptable (foundation metadata concept)
2A2 (AJCC) Acceptable (foundation metadata concept)
2A2 (UICC) Acceptable (foundation metadata concept)
2B (AJCC) Acceptable (foundation metadata concept)
2B (UICC) Acceptable (foundation metadata concept)
2C (AJCC) Acceptable (foundation metadata concept)
2C (UICC) Acceptable (foundation metadata concept)
2D (two dimensional) external beam radiation therapy involves dose calculation without projection onto 3D imaging and delivered without 3D techniques. Preferred (foundation metadata concept)
2D (two dimensional) external beam radiotherapy Acceptable (foundation metadata concept)
2D (two dimensional) mode ultrasound - action Preferred (foundation metadata concept)
2D-EBRT - two dimensional external beam radiation therapy Acceptable (foundation metadata concept)
2E (AJCC) Acceptable (foundation metadata concept)
2E (UICC) Acceptable (foundation metadata concept)
2H post 100 g glucose PO Acceptable (foundation metadata concept)
2H post 75 g glucose PO Acceptable (foundation metadata concept)
2H post dose glucose Acceptable (foundation metadata concept)
2H post incubation Acceptable (foundation metadata concept)
2H post meal Acceptable (foundation metadata concept)
2H post peritoneal dialysis Acceptable (foundation metadata concept)
2H specimen Acceptable (foundation metadata concept)
2H4 Acceptable (foundation metadata concept)
2a Preferred (foundation metadata concept)
2a (qualifier value) Preferred (foundation metadata concept)
2b Preferred (foundation metadata concept)
2b (qualifier value) Preferred (foundation metadata concept)
2g protein exchanges/day Preferred (foundation metadata concept)
2g protein exchanges/day (qualifier value) Preferred (foundation metadata concept)
2g protein exchanges/kg body weight Preferred (foundation metadata concept)
2g protein exchanges/kg body weight (qualifier value) Preferred (foundation metadata concept)
2g protein exchanges/meal Preferred (foundation metadata concept)
2g protein exchanges/meal (qualifier value) Preferred (foundation metadata concept)
2nd Acceptable (foundation metadata concept)
2nd HiB and DTP vaccine given Preferred (foundation metadata concept)
2nd HiB and DTP vaccine given (situation) Preferred (foundation metadata concept)
2nd Hib and DTP vaccine given Preferred (foundation metadata concept)
2nd Japanese encephalitis vaccination Preferred (foundation metadata concept)
2nd Japanese encephalitis vaccination Preferred (foundation metadata concept)
2nd Japanese encephalitis vaccination (procedure) Preferred (foundation metadata concept)
2nd Japanese encephalitis vaccination (procedure) Preferred (foundation metadata concept)
2nd floor Acceptable (foundation metadata concept)
2nd heart sound split Acceptable (foundation metadata concept)
2nd hepatitis A junior vaccination Acceptable (foundation metadata concept)
2nd left lumbar vein Acceptable (foundation metadata concept)
2nd right lumbar vein Acceptable (foundation metadata concept)
2nd specimen Acceptable (foundation metadata concept)
2nd stage of labor length Preferred (foundation metadata concept)
2nd stage of labor length Acceptable (foundation metadata concept)
2nd stage of labour length (observable entity) Preferred (foundation metadata concept)
2nd trimester Acceptable (foundation metadata concept)
2p partial trisomy syndrome Preferred (foundation metadata concept)
2p partial trisomy syndrome (disorder) Preferred (foundation metadata concept)
2p13.2 microdeletion syndrome Preferred (foundation metadata concept)
2p13.2 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
2p15p16.1 microdeletion syndrome Preferred (foundation metadata concept)
2p15p16.1 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
2p15p16.1 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism. Preferred (foundation metadata concept)
2p21 microdeletion syndrome Preferred (foundation metadata concept)
2p21 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
2p21 microdeletion syndrome without cystinuria Preferred (foundation metadata concept)
2p21 microdeletion syndrome without cystinuria (disorder) Preferred (foundation metadata concept)
2p21 microdeletion syndrome without cystinuria is a rare partial autosomal monosomy characterized by weak fetal movements, severe infantile hypotonia and feeding difficulties that spontaneously improve with time, urogenital abnormalities (hypospadias or hypoplastic labia majora), global development delay, mild intellectual disability and facial dysmorphism (dolichocephaly, frontal bossing, bilateral ptosis, midface retrusion, open mouth with tented upper lip vermilion). Affected individuals have borderline elevated serum lactate but no cystinuria. Preferred (foundation metadata concept)
2q partial trisomy syndrome Preferred (foundation metadata concept)
2q partial trisomy syndrome (disorder) Preferred (foundation metadata concept)
2q23.1 microdeletion syndrome Preferred (foundation metadata concept)
2q23.1 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
2q23.1 microduplication syndrome Preferred (foundation metadata concept)
2q23.1 microduplication syndrome (disorder) Preferred (foundation metadata concept)
2q23.1 microduplication syndrome is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the long arm of chromosome 2, primarily characterized by global developmental delay, hypotonia, autistic-like features and behavioral problems. Craniofacial dysmorphism (arched eyebrows, hypertelorism, bilateral ptosis, prominent nose, wide mouth, micro/retrognathia) and an affable personality are also commonly associated. Minor digital anomalies (fifth finger clinodactyly and large, broad first toe) have occasionally been reported. Preferred (foundation metadata concept)
2q24 microdeletion syndrome Preferred (foundation metadata concept)
2q24 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
2q24 microdeletion syndrome is a chromosomal anomaly consisting of a partial long arm deletion of chromosome 2 and characterized clinically by a wide range of manifestations (depending on the specific region deleted) which can include seizures, microcephaly, dysmorphic features, cleft palate, eye abnormalities (coloboma, cataract and microphthalmia), growth retardation, failure to thrive, heart defects, limb anomalies, developmental delay and autism. Preferred (foundation metadata concept)
2q31.1 microdeletion syndrome Preferred (foundation metadata concept)
2q31.1 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
2q31.1 microdeletion syndrome is a well-defined and clinically recognisable syndrome characterized by moderate to severe developmental delay, short stature, facial dysmorphism and variable limb defects. Preferred (foundation metadata concept)
2q32q33 microdeletion syndrome Preferred (foundation metadata concept)
2q32q33 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
2q33.1 microdeletion syndrome Preferred (foundation metadata concept)
2q33.1 microdeletion syndrome (disorder) Preferred (foundation metadata concept)
2q37 deletion syndrome Acceptable (foundation metadata concept)
2x normal saline 1.8% infusion solution bag Acceptable (foundation metadata concept)
2x/wk Acceptable (foundation metadata concept)
3 Preferred (foundation metadata concept)
3 Preferred (foundation metadata concept)
3 (AJCC) Acceptable (foundation metadata concept)
3 (UICC) Acceptable (foundation metadata concept)
3 (qualifier value) Preferred (foundation metadata concept)
3 Buck shot Preferred (foundation metadata concept)
3 Buck shot, device Acceptable (foundation metadata concept)
3 Buck shot, device (qualifier value) Preferred (foundation metadata concept)
3 alpha hydroxycholanic acid Acceptable (foundation metadata concept)

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