900000000000509007: United States of America 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)\US 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
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
467	Preferred (foundation metadata concept)
467 (qualifier value)	Preferred (foundation metadata concept)
469.01	Preferred (foundation metadata concept)
469.01 (qualifier value)	Preferred (foundation metadata concept)
46XX	Preferred (foundation metadata concept)
46XX (qualifier value)	Preferred (foundation metadata concept)
47 (AJCC)	Acceptable (foundation metadata concept)
47 (UICC)	Acceptable (foundation metadata concept)
47,XYY syndrome	Acceptable (foundation metadata concept)
47-Ca	Acceptable (foundation metadata concept)
475	Preferred (foundation metadata concept)
475 (qualifier value)	Preferred (foundation metadata concept)
48	Preferred (foundation metadata concept)
48 (AJCC)	Acceptable (foundation metadata concept)
48 (UICC)	Acceptable (foundation metadata concept)
48 (qualifier value)	Preferred (foundation metadata concept)
48 hour ambulatory electrocardiographic monitoring	Preferred (foundation metadata concept)
48 hour ambulatory electrocardiographic monitoring (procedure)	Preferred (foundation metadata concept)
48 hour fecal specimen	Acceptable (foundation metadata concept)
48 hour stool specimen	Preferred (foundation metadata concept)
48 hour urine specimen	Preferred (foundation metadata concept)
48 hours	Preferred (foundation metadata concept)
48 hours (qualifier value)	Preferred (foundation metadata concept)
48,XYYY syndrome	Preferred (foundation metadata concept)
48,XYYY syndrome (disorder)	Preferred (foundation metadata concept)
48-Cr	Acceptable (foundation metadata concept)
48-V	Acceptable (foundation metadata concept)
48.19	Preferred (foundation metadata concept)
48.19 (qualifier value)	Preferred (foundation metadata concept)
48.2	Preferred (foundation metadata concept)
48.2 (qualifier value)	Preferred (foundation metadata concept)
480	Preferred (foundation metadata concept)
480 (qualifier value)	Preferred (foundation metadata concept)
48000	Preferred (foundation metadata concept)
48000 (qualifier value)	Preferred (foundation metadata concept)
48000000	Preferred (foundation metadata concept)
48000000 (qualifier value)	Preferred (foundation metadata concept)
49 (AJCC)	Acceptable (foundation metadata concept)
49 (UICC)	Acceptable (foundation metadata concept)
49,XXXYY syndrome	Preferred (foundation metadata concept)
49,XXXYY syndrome (disorder)	Preferred (foundation metadata concept)
49,XXXYY syndrome is a rare gonosome anomaly syndrome characterized by a eunuchoid habitus with gynecoid fat distribution and shape, normal to tall stature, moderate to severe intellectual disability, distinctive facial features (e.g. prominent forehead, epicanthic folds, broad nasal bridge, prognathism), gynecomastia, hypogonadism, cryptorchidism, small penis and behavioral abnormalities (including solitary, passive disposition but prone to aggressive outbursts, autistic). Skeletal malformations, such as delayed bone age, fifth finger clinodactyly, elbow malformations and slow molar development, may also be associated.	Preferred (foundation metadata concept)
49,XYYYY syndrome	Preferred (foundation metadata concept)
49,XYYYY syndrome (disorder)	Preferred (foundation metadata concept)
49-V	Acceptable (foundation metadata concept)
493 Poland	Preferred (foundation metadata concept)
4A (AJCC)	Acceptable (foundation metadata concept)
4A (UICC)	Acceptable (foundation metadata concept)
4A1 (AJCC)	Acceptable (foundation metadata concept)
4A1 (UICC)	Acceptable (foundation metadata concept)
4A2 (AJCC)	Acceptable (foundation metadata concept)
4A2 (UICC)	Acceptable (foundation metadata concept)
4B (AJCC)	Acceptable (foundation metadata concept)
4B (UICC)	Acceptable (foundation metadata concept)
4C (AJCC)	Acceptable (foundation metadata concept)
4C (UICC)	Acceptable (foundation metadata concept)
4D (four dimensional) ultrasonography	Acceptable (foundation metadata concept)
4D (four dimensional) ultrasound	Acceptable (foundation metadata concept)
4D (four dimensional) ultrasound scan	Acceptable (foundation metadata concept)
4Fr	Acceptable (foundation metadata concept)
4H leukodystrophy	Preferred (foundation metadata concept)
4H leukodystrophy (disorder)	Preferred (foundation metadata concept)
4H post incubation	Acceptable (foundation metadata concept)
4H post peritoneal dialysis	Acceptable (foundation metadata concept)
4H specimen	Acceptable (foundation metadata concept)
4H specimen	Acceptable (foundation metadata concept)
4H syndrome	Acceptable (foundation metadata concept)
4KB5	Acceptable (foundation metadata concept)
4a	Preferred (foundation metadata concept)
4a-hydroxytetrahydrobiopterin dehydratase	Preferred (foundation metadata concept)
4a-hydroxytetrahydrobiopterin dehydratase (substance)	Preferred (foundation metadata concept)
4ab	Preferred (foundation metadata concept)
4b	Preferred (foundation metadata concept)
4c	Preferred (foundation metadata concept)
4d	Preferred (foundation metadata concept)
4e	Preferred (foundation metadata concept)
4f	Preferred (foundation metadata concept)
4p minus syndrome	Acceptable (foundation metadata concept)
4p partial monosomy syndrome	Preferred (foundation metadata concept)
4p partial monosomy syndrome (disorder)	Preferred (foundation metadata concept)
4p partial trisomy syndrome	Preferred (foundation metadata concept)
4p partial trisomy syndrome (disorder)	Preferred (foundation metadata concept)
4p16.3 microduplication syndrome	Preferred (foundation metadata concept)
4p16.3 microduplication syndrome (disorder)	Preferred (foundation metadata concept)
4p16.3 microduplication syndrome is a rare genetic syndrome that results from the partial duplication of the short arm of chromosome 4. It has a highly variable phenotype, principally characterized by psychomotor and language delay, seizures and dysmorphic features such as high forehead with frontal bossing, hypertelorism, prominent glabella, long narrow palpebral fissures, low set ears and short neck. Eye abnormalities (glaucoma, irregular iris pigmentation, hyperopia) have also been reported.	Preferred (foundation metadata concept)
4q partial monosomy syndrome	Preferred (foundation metadata concept)
4q partial monosomy syndrome (disorder)	Preferred (foundation metadata concept)
4q partial trisomy syndrome	Preferred (foundation metadata concept)
4q partial trisomy syndrome (disorder)	Preferred (foundation metadata concept)
4q21 microdeletion syndrome	Preferred (foundation metadata concept)
4q21 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
4q25 proximal deletion syndrome	Preferred (foundation metadata concept)
4q25 proximal deletion syndrome (disorder)	Preferred (foundation metadata concept)
4th	Acceptable (foundation metadata concept)
4th floor	Acceptable (foundation metadata concept)
4th generation HIV ELISA	Acceptable (foundation metadata concept)
4th left lumbar vein	Acceptable (foundation metadata concept)
4th nerve palsy	Acceptable (foundation metadata concept)
4th right lumbar vein	Acceptable (foundation metadata concept)
4x/wk	Acceptable (foundation metadata concept)
5	Preferred (foundation metadata concept)

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Reference Sets

Reference set descriptor

GB English

US English

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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)