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
107m-Ag	Acceptable (foundation metadata concept)
108	Preferred (foundation metadata concept)
108 (qualifier value)	Preferred (foundation metadata concept)
1080	Preferred (foundation metadata concept)
1080 (qualifier value)	Preferred (foundation metadata concept)
1080 toxicity	Acceptable (foundation metadata concept)
1081 toxicity	Acceptable (foundation metadata concept)
108m-Ag	Acceptable (foundation metadata concept)
109-Cd	Acceptable (foundation metadata concept)
109-In	Acceptable (foundation metadata concept)
109-Pd	Acceptable (foundation metadata concept)
109m-Ag	Acceptable (foundation metadata concept)
10G	Preferred (foundation metadata concept)
10G (qualifier value)	Preferred (foundation metadata concept)
10^12 cells/L	Preferred (foundation metadata concept)
10^12 cells/liter	Acceptable (foundation metadata concept)
10^12 cells/liter (qualifier value)	Preferred (foundation metadata concept)
10^12/L	Preferred (foundation metadata concept)
10^12/liter	Acceptable (foundation metadata concept)
10^12/liter (qualifier value)	Preferred (foundation metadata concept)
10^6 cells/L	Preferred (foundation metadata concept)
10^6 cells/liter	Acceptable (foundation metadata concept)
10^6 cells/liter (qualifier value)	Preferred (foundation metadata concept)
10^6 sperm/ejaculate	Acceptable (foundation metadata concept)
10^6 spermatozoa/ejaculate	Preferred (foundation metadata concept)
10^6 spermatozoa/ejaculate (qualifier value)	Preferred (foundation metadata concept)
10^6/L	Preferred (foundation metadata concept)
10^6/liter	Acceptable (foundation metadata concept)
10^6/liter (qualifier value)	Preferred (foundation metadata concept)
10^9 cells/L	Preferred (foundation metadata concept)
10^9 cells/liter	Acceptable (foundation metadata concept)
10^9 cells/liter (qualifier value)	Preferred (foundation metadata concept)
10^9 platelets/L	Preferred (foundation metadata concept)
10^9 platelets/liter	Acceptable (foundation metadata concept)
10^9 platelets/liter (qualifier value)	Preferred (foundation metadata concept)
10^9/L	Preferred (foundation metadata concept)
10^9/liter	Acceptable (foundation metadata concept)
10^9/liter (qualifier value)	Preferred (foundation metadata concept)
10g carbohydrate exchanges/day	Preferred (foundation metadata concept)
10g carbohydrate exchanges/day (qualifier value)	Preferred (foundation metadata concept)
10g carbohydrate exchanges/in-between meal snack	Preferred (foundation metadata concept)
10g carbohydrate exchanges/in-between meal snack (qualifier value)	Preferred (foundation metadata concept)
10g carbohydrate exchanges/kg body weight	Preferred (foundation metadata concept)
10g carbohydrate exchanges/kg body weight (qualifier value)	Preferred (foundation metadata concept)
10g carbohydrate exchanges/meal	Preferred (foundation metadata concept)
10g carbohydrate exchanges/meal (qualifier value)	Preferred (foundation metadata concept)
10g monofilament sensation L foot abnormal	Preferred (foundation metadata concept)
10g monofilament sensation L foot abnormal	Preferred (foundation metadata concept)
10g monofilament sensation L foot abnormal	Preferred (foundation metadata concept)
10g monofilament sensation L foot abnormal (finding)	Preferred (foundation metadata concept)
10g monofilament sensation L foot abnormal (finding)	Preferred (foundation metadata concept)
10g monofilament sensation L foot abnormal (situation)	Preferred (foundation metadata concept)
10g monofilament sensation L foot normal	Preferred (foundation metadata concept)
10g monofilament sensation L foot normal	Preferred (foundation metadata concept)
10g monofilament sensation L foot normal	Preferred (foundation metadata concept)
10g monofilament sensation L foot normal (finding)	Preferred (foundation metadata concept)
10g monofilament sensation L foot normal (finding)	Preferred (foundation metadata concept)
10g monofilament sensation L foot normal (situation)	Preferred (foundation metadata concept)
10g monofilament sensation R foot abnormal	Preferred (foundation metadata concept)
10g monofilament sensation R foot abnormal	Preferred (foundation metadata concept)
10g monofilament sensation R foot abnormal	Preferred (foundation metadata concept)
10g monofilament sensation R foot abnormal (finding)	Preferred (foundation metadata concept)
10g monofilament sensation R foot abnormal (finding)	Preferred (foundation metadata concept)
10g monofilament sensation R foot abnormal (situation)	Preferred (foundation metadata concept)
10g monofilament sensation R foot normal	Preferred (foundation metadata concept)
10g monofilament sensation R foot normal	Preferred (foundation metadata concept)
10g monofilament sensation R foot normal	Preferred (foundation metadata concept)
10g monofilament sensation R foot normal (finding)	Preferred (foundation metadata concept)
10g monofilament sensation R foot normal (finding)	Preferred (foundation metadata concept)
10g monofilament sensation R foot normal (situation)	Preferred (foundation metadata concept)
10g monofilament sensation absent	Preferred (foundation metadata concept)
10g monofilament sensation absent	Preferred (foundation metadata concept)
10g monofilament sensation absent	Preferred (foundation metadata concept)
10g monofilament sensation absent (finding)	Preferred (foundation metadata concept)
10g monofilament sensation absent (finding)	Preferred (foundation metadata concept)
10g monofilament sensation absent (situation)	Preferred (foundation metadata concept)
10g monofilament sensation present	Preferred (foundation metadata concept)
10g monofilament sensation present	Preferred (foundation metadata concept)
10g monofilament sensation present	Preferred (foundation metadata concept)
10g monofilament sensation present (finding)	Preferred (foundation metadata concept)
10g monofilament sensation present (finding)	Preferred (foundation metadata concept)
10g monofilament sensation present (situation)	Preferred (foundation metadata concept)
10p partial monosomy syndrome	Preferred (foundation metadata concept)
10p partial monosomy syndrome (disorder)	Preferred (foundation metadata concept)
10p partial trisomy syndrome	Preferred (foundation metadata concept)
10p partial trisomy syndrome (disorder)	Preferred (foundation metadata concept)
10p12p11 microdeletion syndrome	Acceptable (foundation metadata concept)
10q partial monosomy	Preferred (foundation metadata concept)
10q partial monosomy (disorder)	Preferred (foundation metadata concept)
10q partial trisomy syndrome	Preferred (foundation metadata concept)
10q partial trisomy syndrome (disorder)	Preferred (foundation metadata concept)
10q22.3q23.3 microdeletion syndrome	Preferred (foundation metadata concept)
10q22.3q23.3 microdeletion syndrome (disorder)	Preferred (foundation metadata concept)
10q22.3q23.3 microdeletion syndrome is a rare partial autosomal monosomy characterized by a mild facial dysmorphism variably including macrocephaly, broad forehead, hypertelorism or hypotelorism, deep-set eyes, upslanting or downslanting palpebral fissures, low-set ears, flat nasal bridge, smooth philtrum, thin upper lip, cleft palate, cerebellar and cardiac malformations, psychomotor development delay, and behavioral abnormalities (attention deficit hyperactivity disorder, autism). Other rare features may include congenital breast aplasia, arachnodactyly, joint hyperlaxity, club feet, feeding difficulties, failure to thrive.	Preferred (foundation metadata concept)
10q22.3q23.3 microduplication syndrome	Preferred (foundation metadata concept)
10q22.3q23.3 microduplication syndrome (disorder)	Preferred (foundation metadata concept)
10q24 microduplication syndrome	Acceptable (foundation metadata concept)
10th floor	Acceptable (foundation metadata concept)
10x/day	Acceptable (foundation metadata concept)
11	Preferred (foundation metadata concept)
11	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)